[ { "page": 1, "items": [ { "page": 1, "type": "TITLE", "location": { "l": 211.68, "t": 672.48, "r": 399.84, "b": 628.8 }, "text": "STARK STATE COLLEGE\nGENERAL SYLLABUS", "reading_order": 0, "level": 1 }, { "page": 1, "type": "TITLE", "location": { "l": 34.08, "t": 590.4, "r": 181.44, "b": 574.08 }, "text": "Course Information", "reading_order": 1, "level": 2 }, { "page": 1, "type": "TEXT", "location": { "l": 33.6, "t": 570.24, "r": 251.04, "b": 541.44 }, "text": "Course Name: Organic Chemistry I\nCourse Number: CHM241", "reading_order": 2 }, { "page": 1, "type": "TITLE", "location": { "l": 34.56, "t": 515.04, "r": 179.28, "b": 498 }, "text": "Required Materials", "reading_order": 3, "level": 2 }, { "page": 1, "type": "LIST_ITEM", "location": { "l": 33.84, "t": 495.12, "r": 546.72, "b": 466.32 }, "text": "Textbook(s): (1) Organic Chemistry 10th ed. By John McMurry. Free access here and in BrightSpace: Organic Chemistry: A Tenth Edition - OpenStax", "links": [ { "uri": "https://openstax.org/details/books/organic-chemistry", "dest": null, "action_type": "/URI", "bbox": [ 33.75, 464.294, 246.224, 479.736 ] } ], "list_id": "L1", "level": 0, "reading_order": 4 }, { "page": 1, "type": "LIST_ITEM", "location": { "l": 33.6, "t": 464.16, "r": 549.12, "b": 434.4 }, "text": "Organic Chemistry Lab Techniques by Lisa Nichols. Free access here and in Brightspace: Organic Chemistry Lab Techniques (Nichols) - Chemistry LibreTexts", "marker": "(2)", "links": [ { "uri": "https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Lab_Techniques_(Nichols)", "dest": null, "action_type": "/URI", "bbox": [ 444.155, 448.852, 578.25, 464.294 ] }, { "uri": "https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Lab_Techniques_(Nichols)", "dest": null, "action_type": "/URI", "bbox": [ 33.75, 433.41, 232.872, 448.852 ] } ], "list_id": "L1", "level": 0, "reading_order": 5 }, { "page": 1, "type": "TEXT", "location": { "l": 34.08, "t": 417.84, "r": 428.4, "b": 403.68 }, "text": "Required Readings: Online HW: Chem21Labs for online HW and timed quizzes", "reading_order": 6 }, { "page": 1, "type": "TEXT", "location": { "l": 32.88, "t": 386.88, "r": 574.56, "b": 279.36 }, "text": "Additional Materials: Lab Manual: Christie and Padias, “Organic Chemistry Manual 2016-17”, Hayden-McNeil, New York, ISBN: 978-0-7380-8920-1. Lab notebook: Scientific laboratory notebook with carbonless duplicate pages from bookstore (preferred). CHM241 notebook may be used Calculator: scientific calculator such as the “TI-30X IIs.” Cell phones will not be permitted during assessments. Splash-proof Safety Googles and Lab Coat (Mandatory and may be purchased at the bookstore) Molecular model set: May be purchased new or used (recommended Molymod MMS-008 Organic Chemistry Molecular Model, Student Set (50 atom parts)) or can be borrowed during the course on a first-come, first-served basis. ChemDraw Software: License will be provided", "reading_order": 7 } ] }, { "page": 2, "items": [ { "page": 2, "type": "TITLE", "location": { "l": 33.84, "t": 753.84, "r": 221.76, "b": 737.28 }, "text": "Course Outline/Calendar", "reading_order": 0, "level": 2 }, { "page": 2, "type": "TEXT", "location": { "l": 33.12, "t": 733.44, "r": 549.6, "b": 704.64 }, "text": "The date of coverage and order of coverage may be modified based on the faculty member and events beyond the control of faculty members that interfere with class times and teaching.", "reading_order": 1 }, { "page": 2, "type": "TEXT", "location": { "l": 34.32, "t": 686.16, "r": 119.52, "b": 675.12 }, "text": "16 Week Calendar", "reading_order": 2 }, { "page": 2, "type": "TABLE", "location": { "l": 34.56, "t": 675.84, "r": 576.96, "b": 285.84 }, "text": "
WeekChapter/Topic/Lab
1Syllabus\nChapter 1 Structure and Bonding
1Chapter 1 Structure and Bonding
2Chapter 2 Polar Covalent Bonds; Acids & Bases
3Chapter 2 Polar Covalent Bonds; Acids & Bases
3Chapter 3 Organic Compounds: Alkanes and Their Stereochemistry
4Chapter 3 Organic Compounds: Alkanes and Their Stereochemistry
4Exam I (Chapters 1-3)
5Chapter 4 Cycloalkanes and Their Stereochemistry
5Chapter 5 Stereochemistry at Tetrahedral Centers
6Chapter 5 Stereochemistry at Tetrahedral Centers
6Chapter 6 Overview of Organic Reactions
7Chapter 6 Overview of Organic Reactions
8Exam II (Chapters 4-6)
9Chapter 7 Alkenes
9Chapter 7 Alkenes
10Chapter 8 Alkenes: Reactions and Synthesis
11Chapter 9 Alkynes: An Introduction to Organic Synthesis
12Exam III (Chapters 8-9)
12Chapter 10 Organohalides
13Chapter 11 Reactions of Alkylhalides: Nucleophilic Substitution and Elimination
14Chapter 12 Structure Determination: Mass Spectrometry and IR Spectroscopy
14Review Chapters 10-12
15Exam 4 (Chapters 10-12)
15Review for Final Exam
16ACS Exam
16Final Exam (Chapters 1-12)
", "rows": [ { "row_index": 0, "location": [ 34.56, 661.3956, 576.96, 675.84 ], "cells": [ { "location": [ 34.56, 661.3956, 305.76, 675.84 ], "text": "Week", "html_text": "Week", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": true, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 661.3956, 576.96, 675.84 ], "text": "Chapter/Topic/Lab", "html_text": "Chapter/Topic/Lab", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": true, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 1, "location": [ 34.56, 646.9511, 576.96, 661.3956 ], "cells": [ { "location": [ 34.56, 646.9511, 305.76, 661.3956 ], "text": "1", "html_text": "1", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 646.9511, 576.96, 661.3956 ], "text": "Syllabus\nChapter 1 Structure and Bonding", "html_text": "Syllabus\nChapter 1 Structure and Bonding", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 2, "location": [ 34.56, 632.5067, 576.96, 646.9511 ], "cells": [ { "location": [ 34.56, 632.5067, 305.76, 646.9511 ], "text": "1", "html_text": "1", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 632.5067, 576.96, 646.9511 ], "text": "Chapter 1 Structure and Bonding", "html_text": "Chapter 1 Structure and Bonding", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 3, "location": [ 34.56, 618.0622, 576.96, 632.5067 ], "cells": [ { "location": [ 34.56, 618.0622, 305.76, 632.5067 ], "text": "2", "html_text": "2", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 618.0622, 576.96, 632.5067 ], "text": "Chapter 2 Polar Covalent Bonds; Acids & Bases", "html_text": "Chapter 2 Polar Covalent Bonds; Acids & Bases", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 4, "location": [ 34.56, 603.6178, 576.96, 618.0622 ], "cells": [ { "location": [ 34.56, 603.6178, 305.76, 618.0622 ], "text": "3", "html_text": "3", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 603.6178, 576.96, 618.0622 ], "text": "Chapter 2 Polar Covalent Bonds; Acids & Bases", "html_text": "Chapter 2 Polar Covalent Bonds; Acids & Bases", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 5, "location": [ 34.56, 589.1733, 576.96, 603.6178 ], "cells": [ { "location": [ 34.56, 589.1733, 305.76, 603.6178 ], "text": "3", "html_text": "3", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 589.1733, 576.96, 603.6178 ], "text": "Chapter 3 Organic Compounds: Alkanes and Their Stereochemistry", "html_text": "Chapter 3 Organic Compounds: Alkanes and Their Stereochemistry", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 6, "location": [ 34.56, 574.7289, 576.96, 589.1733 ], "cells": [ { "location": [ 34.56, 574.7289, 305.76, 589.1733 ], "text": "4", "html_text": "4", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 574.7289, 576.96, 589.1733 ], "text": "Chapter 3 Organic Compounds: Alkanes and Their Stereochemistry", "html_text": "Chapter 3 Organic Compounds: Alkanes and Their Stereochemistry", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 7, "location": [ 34.56, 560.2844, 576.96, 574.7289 ], "cells": [ { "location": [ 34.56, 560.2844, 305.76, 574.7289 ], "text": "4", "html_text": "4", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 560.2844, 576.96, 574.7289 ], "text": "Exam I (Chapters 1-3)", "html_text": "Exam I (Chapters 1-3)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 8, "location": [ 34.56, 545.84, 576.96, 560.2844 ], "cells": [ { "location": [ 34.56, 545.84, 305.76, 560.2844 ], "text": "5", "html_text": "5", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 545.84, 576.96, 560.2844 ], "text": "Chapter 4 Cycloalkanes and Their Stereochemistry", "html_text": "Chapter 4 Cycloalkanes and Their Stereochemistry", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 9, "location": [ 34.56, 531.3956, 576.96, 545.84 ], "cells": [ { "location": [ 34.56, 531.3956, 305.76, 545.84 ], "text": "5", "html_text": "5", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 531.3956, 576.96, 545.84 ], "text": "Chapter 5 Stereochemistry at Tetrahedral Centers", "html_text": "Chapter 5 Stereochemistry at Tetrahedral Centers", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 10, "location": [ 34.56, 516.9511, 576.96, 531.3956 ], "cells": [ { "location": [ 34.56, 516.9511, 305.76, 531.3956 ], "text": "6", "html_text": "6", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 516.9511, 576.96, 531.3956 ], "text": "Chapter 5 Stereochemistry at Tetrahedral Centers", "html_text": "Chapter 5 Stereochemistry at Tetrahedral Centers", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 11, "location": [ 34.56, 502.5067, 576.96, 516.9511 ], "cells": [ { "location": [ 34.56, 502.5067, 305.76, 516.9511 ], "text": "6", "html_text": "6", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 502.5067, 576.96, 516.9511 ], "text": "Chapter 6 Overview of Organic Reactions", "html_text": "Chapter 6 Overview of Organic Reactions", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 12, "location": [ 34.56, 488.0622, 576.96, 502.5067 ], "cells": [ { "location": [ 34.56, 488.0622, 305.76, 502.5067 ], "text": "7", "html_text": "7", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 488.0622, 576.96, 502.5067 ], "text": "Chapter 6 Overview of Organic Reactions", "html_text": "Chapter 6 Overview of Organic Reactions", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 13, "location": [ 34.56, 473.6178, 576.96, 488.0622 ], "cells": [ { "location": [ 34.56, 473.6178, 305.76, 488.0622 ], "text": "8", "html_text": "8", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 473.6178, 576.96, 488.0622 ], "text": "Exam II (Chapters 4-6)", "html_text": "Exam II (Chapters 4-6)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 14, "location": [ 34.56, 459.1733, 576.96, 473.6178 ], "cells": [ { "location": [ 34.56, 459.1733, 305.76, 473.6178 ], "text": "9", "html_text": "9", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 459.1733, 576.96, 473.6178 ], "text": "Chapter 7 Alkenes", "html_text": "Chapter 7 Alkenes", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 15, "location": [ 34.56, 444.7289, 576.96, 459.1733 ], "cells": [ { "location": [ 34.56, 444.7289, 305.76, 459.1733 ], "text": "9", "html_text": "9", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 444.7289, 576.96, 459.1733 ], "text": "Chapter 7 Alkenes", "html_text": "Chapter 7 Alkenes", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 16, "location": [ 34.56, 430.2844, 576.96, 444.7289 ], "cells": [ { "location": [ 34.56, 430.2844, 305.76, 444.7289 ], "text": "10", "html_text": "10", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 430.2844, 576.96, 444.7289 ], "text": "Chapter 8 Alkenes: Reactions and Synthesis", "html_text": "Chapter 8 Alkenes: Reactions and Synthesis", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 17, "location": [ 34.56, 415.84, 576.96, 430.2844 ], "cells": [ { "location": [ 34.56, 415.84, 305.76, 430.2844 ], "text": "11", "html_text": "11", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 415.84, 576.96, 430.2844 ], "text": "Chapter 9 Alkynes: An Introduction to Organic Synthesis", "html_text": "Chapter 9 Alkynes: An Introduction to Organic Synthesis", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 18, "location": [ 34.56, 401.3956, 576.96, 415.84 ], "cells": [ { "location": [ 34.56, 401.3956, 305.76, 415.84 ], "text": "12", "html_text": "12", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 401.3956, 576.96, 415.84 ], "text": "Exam III (Chapters 8-9)", "html_text": "Exam III (Chapters 8-9)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 19, "location": [ 34.56, 386.9511, 576.96, 401.3956 ], "cells": [ { "location": [ 34.56, 386.9511, 305.76, 401.3956 ], "text": "12", "html_text": "12", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 386.9511, 576.96, 401.3956 ], "text": "Chapter 10 Organohalides", "html_text": "Chapter 10 Organohalides", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 20, "location": [ 34.56, 372.5067, 576.96, 386.9511 ], "cells": [ { "location": [ 34.56, 372.5067, 305.76, 386.9511 ], "text": "13", "html_text": "13", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 372.5067, 576.96, 386.9511 ], "text": "Chapter 11 Reactions of Alkylhalides: Nucleophilic Substitution and Elimination", "html_text": "Chapter 11 Reactions of Alkylhalides: Nucleophilic Substitution and Elimination", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 21, "location": [ 34.56, 358.0622, 576.96, 372.5067 ], "cells": [ { "location": [ 34.56, 358.0622, 305.76, 372.5067 ], "text": "14", "html_text": "14", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 358.0622, 576.96, 372.5067 ], "text": "Chapter 12 Structure Determination: Mass Spectrometry and IR Spectroscopy", "html_text": "Chapter 12 Structure Determination: Mass Spectrometry and IR Spectroscopy", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 22, "location": [ 34.56, 343.6178, 576.96, 358.0622 ], "cells": [ { "location": [ 34.56, 343.6178, 305.76, 358.0622 ], "text": "14", "html_text": "14", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 343.6178, 576.96, 358.0622 ], "text": "Review Chapters 10-12", "html_text": "Review Chapters 10-12", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 23, "location": [ 34.56, 329.1733, 576.96, 343.6178 ], "cells": [ { "location": [ 34.56, 329.1733, 305.76, 343.6178 ], "text": "15", "html_text": "15", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 329.1733, 576.96, 343.6178 ], "text": "Exam 4 (Chapters 10-12)", "html_text": "Exam 4 (Chapters 10-12)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 24, "location": [ 34.56, 314.7289, 576.96, 329.1733 ], "cells": [ { "location": [ 34.56, 314.7289, 305.76, 329.1733 ], "text": "15", "html_text": "15", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 314.7289, 576.96, 329.1733 ], "text": "Review for Final Exam", "html_text": "Review for Final Exam", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 25, "location": [ 34.56, 300.2844, 576.96, 314.7289 ], "cells": [ { "location": [ 34.56, 300.2844, 305.76, 314.7289 ], "text": "16", "html_text": "16", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 300.2844, 576.96, 314.7289 ], "text": "ACS Exam", "html_text": "ACS Exam", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 26, "location": [ 34.56, 285.84, 576.96, 300.2844 ], "cells": [ { "location": [ 34.56, 285.84, 305.76, 300.2844 ], "text": "16", "html_text": "16", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 305.76, 285.84, 576.96, 300.2844 ], "text": "Final Exam (Chapters 1-12)", "html_text": "Final Exam (Chapters 1-12)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" } ], "n_rows": 27, "n_cols": 2, "ref": "#/tables/0", "reading_order": 3 } ] }, { "page": 3, "items": [ { "page": 3, "type": "TEXT", "location": { "l": 34.56, "t": 752.88, "r": 191.52, "b": 738 }, "text": "LABORATORY SCHEDULE", "reading_order": 0 }, { "page": 3, "type": "TABLE", "location": { "l": 34.8, "t": 737.04, "r": 577.44, "b": 219.84 }, "text": "
WeekExperiment Number, Name and Lab Manual Reference (#A/B)Description
10 - Welcome• Safety Training\\n• Introduction to ChemDraw\\n• Lab equipment and procedures\\n• Molecular models\\n• Notebook primer
2N/ASkills Academy Session #2 @ 10:00-12:20 H205\\nNomenclature, Lewis Structure, Formal Charge workshop – All lab groups invited to attend
31 – Common Procedures (4A)• Recrystallization\\n• Filtration\\n• Melting Point Determination
42 – TLC and IR spectroscopy (1A and 2A)• Thin layer chromatography and\\n• Infrared spectroscopy analysis of analgesic drugs
53 – Extraction and Purification (3A)• Extraction and purification of spinach pigments\\n• Column chromatography\\n• Introduction to rotary evaporation
64 – Steam Distillation – Isolation of Limonene from Citrus Fruit (6A)• Extraction of limonene\\n• Simple vs. fractional distillation\\n• Stereochemistry and polarimetry
75 – Spectral Analysis Methods• Spectral analysis methods: IR, NMR, MS
85 – Spectral Analysis Working Day• Spectral analysis workshop\\n• (attendance required)\\nSkills Academy Session #4 @8:30-10:00 H205
96 – Extraction and Sublimation (5A)• Extraction of caffeine from tea\\n• Isolation of caffeine\\n• Analysis by IR and GC-MS
107 – Hydrogenation of Methyl Oleate (12A)• Catalytic reduction of methyl oleate\\n• Isolation and characterization of methyl stearate
118 – Synthesis of Esters (8A)• Reactions of alcohols - esterification\\n• Purification by simple distillation
129 – NMR Analysis and Diels Alder Reaction (4B)• Matching H1 NMR spectra with structures\\n• Diels Alder cycloaddition of olefins
1310 – SN1 and SN2Reactions (10A)• Reactions of alkyl halides by SN1 and SN2
1411 – oxidation rxn and GC-MS (2B)• Green oxidation of alcohols\\n• Synthesis of camphor by oxidation of borneol\\n• Analysis by GC-MS
15Lab Practical• Lab practical and written components\\n• Chapters 12 and 13 included
", "rows": [ { "row_index": 0, "location": [ 34.8, 704.715, 577.44, 737.04 ], "cells": [ { "location": [ 34.8, 704.715, 215.68, 737.04 ], "text": "Week", "html_text": "Week", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": true, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 704.715, 396.56, 737.04 ], "text": "Experiment Number, Name and Lab Manual Reference (#A/B)", "html_text": "Experiment Number, Name and Lab Manual Reference (#A/B)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": true, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 704.715, 577.44, 737.04 ], "text": "Description", "html_text": "Description", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": true, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 1, "location": [ 34.8, 672.39, 577.44, 704.715 ], "cells": [ { "location": [ 34.8, 672.39, 215.68, 704.715 ], "text": "1", "html_text": "1", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 672.39, 396.56, 704.715 ], "text": "0 - Welcome", "html_text": "0 - Welcome", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 672.39, 577.44, 704.715 ], "text": "• Safety Training\n• Introduction to ChemDraw\n• Lab equipment and procedures\n• Molecular models\n• Notebook primer", "html_text": "• Safety Training\n• Introduction to ChemDraw\n• Lab equipment and procedures\n• Molecular models\n• Notebook primer", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 2, "location": [ 34.8, 640.065, 577.44, 672.39 ], "cells": [ { "location": [ 34.8, 640.065, 215.68, 672.39 ], "text": "2", "html_text": "2", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 640.065, 396.56, 672.39 ], "text": "N/A", "html_text": "N/A", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 640.065, 577.44, 672.39 ], "text": "Skills Academy Session #2 @ 10:00-12:20 H205\nNomenclature, Lewis Structure, Formal Charge workshop – All lab groups invited to attend", "html_text": "Skills Academy Session #2 @ 10:00-12:20 H205\nNomenclature, Lewis Structure, Formal Charge workshop – All lab groups invited to attend", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 3, "location": [ 34.8, 607.74, 577.44, 640.065 ], "cells": [ { "location": [ 34.8, 607.74, 215.68, 640.065 ], "text": "3", "html_text": "3", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 607.74, 396.56, 640.065 ], "text": "1 – Common Procedures (4A)", "html_text": "1 – Common Procedures (4A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 607.74, 577.44, 640.065 ], "text": "• Recrystallization\n• Filtration\n• Melting Point Determination", "html_text": "• Recrystallization\n• Filtration\n• Melting Point Determination", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 4, "location": [ 34.8, 575.415, 577.44, 607.74 ], "cells": [ { "location": [ 34.8, 575.415, 215.68, 607.74 ], "text": "4", "html_text": "4", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 575.415, 396.56, 607.74 ], "text": "2 – TLC and IR spectroscopy (1A and 2A)", "html_text": "2 – TLC and IR spectroscopy (1A and 2A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 575.415, 577.44, 607.74 ], "text": "• Thin layer chromatography and\n• Infrared spectroscopy analysis of analgesic drugs", "html_text": "• Thin layer chromatography and\n• Infrared spectroscopy analysis of analgesic drugs", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 5, "location": [ 34.8, 543.09, 577.44, 575.415 ], "cells": [ { "location": [ 34.8, 543.09, 215.68, 575.415 ], "text": "5", "html_text": "5", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 543.09, 396.56, 575.415 ], "text": "3 – Extraction and Purification (3A)", "html_text": "3 – Extraction and Purification (3A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 543.09, 577.44, 575.415 ], "text": "• Extraction and purification of spinach pigments\n• Column chromatography\n• Introduction to rotary evaporation", "html_text": "• Extraction and purification of spinach pigments\n• Column chromatography\n• Introduction to rotary evaporation", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 6, "location": [ 34.8, 510.765, 577.44, 543.09 ], "cells": [ { "location": [ 34.8, 510.765, 215.68, 543.09 ], "text": "6", "html_text": "6", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 510.765, 396.56, 543.09 ], "text": "4 – Steam Distillation – Isolation of Limonene from Citrus Fruit (6A)", "html_text": "4 – Steam Distillation – Isolation of Limonene from Citrus Fruit (6A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 510.765, 577.44, 543.09 ], "text": "• Extraction of limonene\n• Simple vs. fractional distillation\n• Stereochemistry and polarimetry", "html_text": "• Extraction of limonene\n• Simple vs. fractional distillation\n• Stereochemistry and polarimetry", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 7, "location": [ 34.8, 478.44, 577.44, 510.765 ], "cells": [ { "location": [ 34.8, 478.44, 215.68, 510.765 ], "text": "7", "html_text": "7", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 478.44, 396.56, 510.765 ], "text": "5 – Spectral Analysis Methods", "html_text": "5 – Spectral Analysis Methods", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 478.44, 577.44, 510.765 ], "text": "• Spectral analysis methods: IR, NMR, MS", "html_text": "• Spectral analysis methods: IR, NMR, MS", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 8, "location": [ 34.8, 446.115, 577.44, 478.44 ], "cells": [ { "location": [ 34.8, 446.115, 215.68, 478.44 ], "text": "8", "html_text": "8", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 446.115, 396.56, 478.44 ], "text": "5 – Spectral Analysis Working Day", "html_text": "5 – Spectral Analysis Working Day", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 446.115, 577.44, 478.44 ], "text": "• Spectral analysis workshop\n• (attendance required)\nSkills Academy Session #4 @8:30-10:00 H205", "html_text": "• Spectral analysis workshop\n• (attendance required)\nSkills Academy Session #4 @8:30-10:00 H205", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 9, "location": [ 34.8, 413.79, 577.44, 446.115 ], "cells": [ { "location": [ 34.8, 413.79, 215.68, 446.115 ], "text": "9", "html_text": "9", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 413.79, 396.56, 446.115 ], "text": "6 – Extraction and Sublimation (5A)", "html_text": "6 – Extraction and Sublimation (5A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 413.79, 577.44, 446.115 ], "text": "• Extraction of caffeine from tea\n• Isolation of caffeine\n• Analysis by IR and GC-MS", "html_text": "• Extraction of caffeine from tea\n• Isolation of caffeine\n• Analysis by IR and GC-MS", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 10, "location": [ 34.8, 381.465, 577.44, 413.79 ], "cells": [ { "location": [ 34.8, 381.465, 215.68, 413.79 ], "text": "10", "html_text": "10", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 381.465, 396.56, 413.79 ], "text": "7 – Hydrogenation of Methyl Oleate (12A)", "html_text": "7 – Hydrogenation of Methyl Oleate (12A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 381.465, 577.44, 413.79 ], "text": "• Catalytic reduction of methyl oleate\n• Isolation and characterization of methyl stearate", "html_text": "• Catalytic reduction of methyl oleate\n• Isolation and characterization of methyl stearate", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 11, "location": [ 34.8, 349.14, 577.44, 381.465 ], "cells": [ { "location": [ 34.8, 349.14, 215.68, 381.465 ], "text": "11", "html_text": "11", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 349.14, 396.56, 381.465 ], "text": "8 – Synthesis of Esters (8A)", "html_text": "8 – Synthesis of Esters (8A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 349.14, 577.44, 381.465 ], "text": "• Reactions of alcohols - esterification\n• Purification by simple distillation", "html_text": "• Reactions of alcohols - esterification\n• Purification by simple distillation", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 12, "location": [ 34.8, 316.815, 577.44, 349.14 ], "cells": [ { "location": [ 34.8, 316.815, 215.68, 349.14 ], "text": "12", "html_text": "12", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 316.815, 396.56, 349.14 ], "text": "9 – NMR Analysis and Diels Alder Reaction (4B)", "html_text": "9 – NMR Analysis and Diels Alder Reaction (4B)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 316.815, 577.44, 349.14 ], "text": "• Matching H1 NMR spectra with structures\\n• Diels Alder cycloaddition of olefins", "html_text": "• Matching H1 NMR spectra with structures\\n• Diels Alder cycloaddition of olefins", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 13, "location": [ 34.8, 284.49, 577.44, 316.815 ], "cells": [ { "location": [ 34.8, 284.49, 215.68, 316.815 ], "text": "13", "html_text": "13", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 284.49, 396.56, 316.815 ], "text": "10 – SN1 and SN2Reactions (10A)", "html_text": "10 – SN1 and SN2Reactions (10A)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 284.49, 577.44, 316.815 ], "text": "• Reactions of alkyl halides by SN1 and SN2", "html_text": "• Reactions of alkyl halides by SN1 and SN2", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 14, "location": [ 34.8, 252.165, 577.44, 284.49 ], "cells": [ { "location": [ 34.8, 252.165, 215.68, 284.49 ], "text": "14", "html_text": "14", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 252.165, 396.56, 284.49 ], "text": "11 – oxidation rxn and GC-MS (2B)", "html_text": "11 – oxidation rxn and GC-MS (2B)", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 252.165, 577.44, 284.49 ], "text": "• Green oxidation of alcohols\n• Synthesis of camphor by oxidation of borneol\n• Analysis by GC-MS", "html_text": "• Green oxidation of alcohols\n• Synthesis of camphor by oxidation of borneol\n• Analysis by GC-MS", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" }, { "row_index": 15, "location": [ 34.8, 219.84, 577.44, 252.165 ], "cells": [ { "location": [ 34.8, 219.84, 215.68, 252.165 ], "text": "15", "html_text": "15", "links": [], "cell_header_index": 0, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 215.68, 219.84, 396.56, 252.165 ], "text": "Lab Practical", "html_text": "Lab Practical", "links": [], "cell_header_index": 1, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" }, { "location": [ 396.56, 219.84, 577.44, 252.165 ], "text": "• Lab practical and written components\n• Chapters 12 and 13 included", "html_text": "• Lab practical and written components\n• Chapters 12 and 13 included", "links": [], "cell_header_index": 2, "rowspan": 1, "colspan": 1, "column_header": false, "row_header": false, "placeholder": false, "ref": "#/tables/0" } ], "ref": "#/tables/0" } ], "n_rows": 16, "n_cols": 3, "ref": "#/tables/0", "reading_order": 1 } ] } ]