{ "document_id": 12598, "filename": "CHM242_Organic-Chemistry-II-artifacted.pdf", "engine": "paddleocr_vl", "source_run_id": 12709, "generated_at": "2026-11-03T00:11:43+00:00", "page_count": 3, "counts_by_type": { "figure": 1, "footer": 6, "header": 1, "heading": 2, "link": 3, "table": 2, "table_cell": 45, "text": 7, "title": 1 }, "timings": { "total_ms": 1445, "structure_ms": 207, "text_layer_ms": 14, "build_ms": 13 }, "pages": [ { "document_id": 12598, "page": 1, "width": 612, "height": 792, "rotation": 0, "pipeline_version": "paddleocr-vl-1.6+paul-48", "width_pt": 612, "height_pt": 792, "engine": "paddleocr_vl", "source_run_id": 12709, "item_count": 14, "counts_by_type": { "figure": 1, "footer": 2, "heading": 1, "link": 3, "text": 6, "title": 1 }, "build_ms": 3, "items": [ { "id": "p1.1", "order": 1, "type": "figure", "bbox": { "l": 33.6, "t": 760.08, "r": 170.16, "b": 673.2 }, "text": "", "attrs": { "role": "page_header", "block_label": "header_image" }, "reading_order": 0 }, { "id": "p1.2", "order": 2, "type": "title", "bbox": { "l": 211.68, "t": 672.48, "r": 399.84, "b": 628.8 }, "text": "STARK STATE COLLEGE\nGENERAL SYLLABUS", "attrs": { "block_label": "doc_title" }, "level": 2, "reading_order": 1 }, { "id": "p1.3", "order": 3, "type": "text", "bbox": { "l": 33.6, "t": 589.44, "r": 254.4, "b": 540.48 }, "text": "Course Information\nCourse Name: Organic Chemistry II\nCourse Number: CHM242", "reading_order": 2 }, { "id": "p1.4", "order": 4, "type": "heading", "bbox": { "l": 34.32, "t": 515.04, "r": 179.28, "b": 498 }, "text": "Required Materials", "attrs": { "block_label": "paragraph_title" }, "level": 3, "reading_order": 3 }, { "id": "p1.5", "order": 5, "type": "text", "bbox": { "l": 33.84, "t": 495.12, "r": 546.72, "b": 466.32 }, "text": "Textbook(s): (1) Organic Chemistry[p1.5.2] ed. By John McMurry. Free access here and in BrightSpace: Organic Chemistry: A Tenth Edition - OpenStax", "children": [ { "id": "p1.5.1", "order": 6, "type": "link", "bbox": { "l": 33.75, "t": 479.736, "r": 246.224, "b": 464.294 }, "text": "Organic Chemistry: A Tenth Edition - OpenStax", "attrs": { "uri": "https://openstax.org/details/books/organic-chemistry", "action_type": "/URI" }, "reading_order": 0 }, { "id": "p1.5.2", "order": 7, "type": "text", "bbox": { "l": 33.84, "t": 495.12, "r": 546.72, "b": 466.32 }, "text": "10^{th}", "attrs": { "inline": true, "text_offset": 34, "text_span": 8, "bbox_estimated": true }, "reading_order": 1 } ], "reading_order": 4 }, { "id": "p1.6", "order": 8, "type": "text", "bbox": { "l": 33.6, "t": 464.16, "r": 549.12, "b": 434.4 }, "text": "(2) Organic Chemistry Lab Techniques by Lisa Nichols. Free access here and in Brightspace: Organic Chemistry Lab Techniques (Nichols) - Chemistry LibreTexts", "children": [ { "id": "p1.6.1", "order": 9, "type": "link", "bbox": { "l": 444.155, "t": 464.294, "r": 578.25, "b": 448.852 }, "text": "Organic Chemistry Lab", "attrs": { "uri": "https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Lab_Techniques_(Nichols)", "action_type": "/URI" }, "reading_order": 0 }, { "id": "p1.6.2", "order": 10, "type": "link", "bbox": { "l": 33.75, "t": 448.852, "r": 232.872, "b": 433.41 }, "text": "Techniques (Nichols) - Chemistry LibreTexts", "attrs": { "uri": "https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Lab_Techniques_(Nichols)", "action_type": "/URI" }, "reading_order": 1 } ], "reading_order": 5 }, { "id": "p1.7", "order": 11, "type": "text", "bbox": { "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 }, { "id": "p1.8", "order": 12, "type": "text", "bbox": { "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 }, { "id": "p1.9", "order": 13, "type": "footer", "bbox": { "l": 34.32, "t": 62.16, "r": 86.64, "b": 48.96 }, "text": "Page 1 of 3", "attrs": { "block_label": "number" }, "reading_order": 8 }, { "id": "p1.10", "order": 14, "type": "footer", "bbox": { "l": 502.08, "t": 61.2, "r": 553.44, "b": 50.16 }, "text": "Rev. 05/2025", "attrs": { "block_label": "footer" }, "reading_order": 9 } ] }, { "document_id": 12598, "page": 2, "width": 612, "height": 792, "rotation": 0, "pipeline_version": "paddleocr-vl-1.6+paul-48", "width_pt": 612, "height_pt": 792, "engine": "paddleocr_vl", "source_run_id": 12709, "item_count": 11, "counts_by_type": { "footer": 2, "heading": 1, "table": 1, "table_cell": 6, "text": 1 }, "build_ms": 3, "items": [ { "id": "p2.1", "order": 1, "type": "heading", "bbox": { "l": 33.84, "t": 753.84, "r": 221.76, "b": 737.28 }, "text": "Course Outline/Calendar", "attrs": { "block_label": "paragraph_title" }, "level": 3, "reading_order": 0 }, { "id": "p2.2", "order": 2, "type": "text", "bbox": { "l": 33.12, "t": 733.68, "r": 549.36, "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 }, { "id": "p2.3", "order": 3, "type": "table", "bbox": { "l": 34.56, "t": 691.68, "r": 577.44, "b": 231.6 }, "text": "", "attrs": { "block_label": "table", "n_rows": 3, "n_cols": 2, "integrity": { "cells_checked": 6, "cells_flagged": 0 } }, "children": [ { "id": "p2.3.1", "order": 4, "type": "table_cell", "bbox": { "l": 41.6398, "t": 687.2709600000001, "r": 65.500119, "b": 665.54712 }, "text": "Week\n1", "attrs": { "row": 0, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 0 }, { "id": "p2.3.2", "order": 5, "type": "table_cell", "bbox": { "l": 126.84, "t": 687.2709600000001, "r": 275.744143, "b": 651.07468 }, "text": "Chapter/Topic/Lab\nSyllabus\\nChapter 16 Aromatic Compounds", "attrs": { "row": 0, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 1 }, { "id": "p2.3.3", "order": 6, "type": "table_cell", "bbox": { "l": 41.6398, "t": 647.10132, "r": 46.68952, "b": 554.6671200000001 }, "text": "1\n2\n3\n3\n4\n4\n5", "attrs": { "row": 1, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 2 }, { "id": "p2.3.4", "order": 7, "type": "table_cell", "bbox": { "l": 126.84, "t": 647.03568, "r": 333.461745, "b": 553.6348800000001 }, "text": "Chapter 16 Aromatic Compounds\nChapter 17 Reactions of Aromatic Compounds\nChapter 17 Reactions of Aromatic Compounds\nReview for Exam 1\nExam I (Chapters 16 & 17)\nChapter 18 Ketones and Aldehydes\nChapter 18 Ketones and Aldehydes", "attrs": { "row": 1, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 3 }, { "id": "p2.3.5", "order": 8, "type": "table_cell", "bbox": { "l": 41.6398, "t": 537.42132, "r": 51.72928, "b": 236.06712000000005 }, "text": "5\n6\n6\n7\n7\n8\n8\n9\n9\n10\n10\n11\n11\n12\n12\n13\n13\n14\n14\n15\n15\n16", "attrs": { "row": 2, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 4 }, { "id": "p2.3.6", "order": 9, "type": "table_cell", "bbox": { "l": 126.84, "t": 537.35568, "r": 336.94026, "b": 235.03488000000004 }, "text": "Chapter 19 Amines\nChapter 19 Amines\nChapter 19 Amines\nExam II (Chapters 18 & 19)\nChapter 20 Carboxylic Acids\nChapter 20 Carboxylic Acids\nChapter 21 Carboxylic Acid Derivatives\nChapter 21 Carboxylic Acid Derivatives\nReview Exam III\nExam III (Chapters 20 & 21)\nChapter 22 Condensation Rxns\nChapter 22 Condensation Rxns\nChapter 22 Condensation Rxns\nChapter 24 Amino Acids, Peptides and Proteins\nChapter 24 Amino Acids, Peptides and Proteins\nChapter 26 Polymers\nReview Exam IV\nExam IV (Chapters 22, 24 & 26)\nReview for ACS full year national exam\nReview for CHM242 Final Exam\nReview for CHM242 Final Exam\nFinal Exam Part 1 CHM242 Final Exam", "attrs": { "row": 2, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 5 } ], "reading_order": 2 }, { "id": "p2.4", "order": 10, "type": "footer", "bbox": { "l": 34.32, "t": 62.16, "r": 86.64, "b": 49.2 }, "text": "Page 2 of 3", "attrs": { "block_label": "number" }, "reading_order": 3 }, { "id": "p2.5", "order": 11, "type": "footer", "bbox": { "l": 502.08, "t": 60.72, "r": 553.44, "b": 50.16 }, "text": "Rev. 05/2025", "attrs": { "block_label": "footer" }, "reading_order": 4 } ] }, { "document_id": 12598, "page": 3, "width": 612, "height": 792, "rotation": 0, "pipeline_version": "paddleocr-vl-1.6+paul-48", "width_pt": 612, "height_pt": 792, "engine": "paddleocr_vl", "source_run_id": 12709, "item_count": 43, "counts_by_type": { "footer": 2, "header": 1, "table": 1, "table_cell": 39 }, "build_ms": 7, "items": [ { "id": "p3.1", "order": 1, "type": "header", "bbox": { "l": 34.56, "t": 755.04, "r": 134.88, "b": 743.04 }, "text": "Laboratory Schedule:", "attrs": { "block_label": "figure_title" }, "level": 2, "reading_order": 0 }, { "id": "p3.2", "order": 2, "type": "table", "bbox": { "l": 34.8, "t": 742.8, "r": 577.2, "b": 176.4 }, "text": "", "attrs": { "block_label": "table", "n_rows": 13, "n_cols": 3, "integrity": { "cells_checked": 39, "cells_flagged": 0 } }, "children": [ { "id": "p3.2.1", "order": 3, "type": "table_cell", "bbox": { "l": 41.6398, "t": 739.65504, "r": 67.939154, "b": 715.75488 }, "text": "Week\n1", "attrs": { "row": 0, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 0 }, { "id": "p3.2.2", "order": 4, "type": "table_cell", "bbox": { "l": 117.84, "t": 739.65504, "r": 259.849752, "b": 729.67488 }, "text": "Experiment Number and Name", "attrs": { "row": 0, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true, "column_header": true, "header_source": "pdf" }, "reading_order": 1 }, { "id": "p3.2.3", "order": 5, "type": "table_cell", "bbox": { "l": 324.84, "t": 739.65504, "r": 517.538307, "b": 659.11488 }, "text": "Description\n• Safety training and model kit check out\\n• Spectroscopy review (2 handouts)\\n• Acid / Base review (1 handout)\\n• Resonance review (1 handout)\\n• Record keeping and literature searches", "attrs": { "row": 0, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true, "column_header": true, "header_source": "pdf" }, "reading_order": 2 }, { "id": "p3.2.4", "order": 6, "type": "table_cell", "bbox": { "l": 41.6398, "t": 655.07568, "r": 47.23708, "b": 645.19488 }, "text": "2", "attrs": { "row": 1, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 3 }, { "id": "p3.2.5", "order": 7, "type": "table_cell", "bbox": { "l": 117.84, "t": 655.07568, "r": 287.169617, "b": 645.19488 }, "text": "5b Electrophilic Aromatic Substitution", "attrs": { "row": 1, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 4 }, { "id": "p3.2.6", "order": 8, "type": "table_cell", "bbox": { "l": 342.8398, "t": 654.47568, "r": 526.895999, "b": 616.51488 }, "text": "• Perform nitration\\n• Practice working with concentrated acids\\n• Determine purity of the product", "attrs": { "row": 1, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 5 }, { "id": "p3.2.7", "order": 9, "type": "table_cell", "bbox": { "l": 41.6398, "t": 612.57504, "r": 47.23708, "b": 602.59488 }, "text": "3", "attrs": { "row": 2, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 6 }, { "id": "p3.2.8", "order": 10, "type": "table_cell", "bbox": { "l": 117.84, "t": 612.57504, "r": 255.307148, "b": 602.59488 }, "text": "Capstone Project Introduction", "attrs": { "row": 2, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 7 }, { "id": "p3.2.9", "order": 11, "type": "table_cell", "bbox": { "l": 342.84003, "t": 612.09504, "r": 493.724733, "b": 574.0348799999999 }, "text": "• Searching the chemical literature\\n• Topic selection\\n• Chemical abstracts research", "attrs": { "row": 2, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 8 }, { "id": "p3.2.10", "order": 12, "type": "table_cell", "bbox": { "l": 41.6398, "t": 569.99568, "r": 47.23708, "b": 560.11488 }, "text": "4", "attrs": { "row": 3, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 9 }, { "id": "p3.2.11", "order": 13, "type": "table_cell", "bbox": { "l": 117.84, "t": 569.99568, "r": 240.582014, "b": 560.11488 }, "text": "6b Aldehydes and ketones", "attrs": { "row": 3, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 10 }, { "id": "p3.2.12", "order": 14, "type": "table_cell", "bbox": { "l": 342.8398, "t": 569.39568, "r": 562.904991, "b": 545.47488 }, "text": "• Identify unknowns\\n• Run more specific aldehyde and ketone reactions", "attrs": { "row": 3, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 11 }, { "id": "p3.2.13", "order": 15, "type": "table_cell", "bbox": { "l": 41.6398, "t": 541.53504, "r": 47.23708, "b": 531.55488 }, "text": "5", "attrs": { "row": 4, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 12 }, { "id": "p3.2.14", "order": 16, "type": "table_cell", "bbox": { "l": 117.84, "t": 541.53504, "r": 231.710338, "b": 531.55488 }, "text": "Wk 5/6 Capstone Project", "attrs": { "row": 4, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 13 }, { "id": "p3.2.15", "order": 17, "type": "table_cell", "bbox": { "l": 342.8398, "t": 540.93504, "r": 488.960381, "b": 502.99488 }, "text": "• Reaction proposals\\n• Inventory check\\n• Collecting and ordering supplies", "attrs": { "row": 4, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 14 }, { "id": "p3.2.16", "order": 18, "type": "table_cell", "bbox": { "l": 41.6398, "t": 498.95568, "r": 47.23708, "b": 489.07488 }, "text": "6", "attrs": { "row": 5, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 15 }, { "id": "p3.2.17", "order": 19, "type": "table_cell", "bbox": { "l": 117.84, "t": 498.95568, "r": 262.877591, "b": 489.07488 }, "text": "11b Synthesis of Methyl Orange", "attrs": { "row": 5, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 16 }, { "id": "p3.2.18", "order": 20, "type": "table_cell", "bbox": { "l": 342.84003, "t": 498.35568, "r": 558.198338, "b": 460.39488 }, "text": "• Perform azo coupling\\n• Observe interaction of dye with different fabrics\\n• Learn about bleaching", "attrs": { "row": 5, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 17 }, { "id": "p3.2.19", "order": 21, "type": "table_cell", "bbox": { "l": 41.6398, "t": 456.35568, "r": 47.23708, "b": 446.47488 }, "text": "7", "attrs": { "row": 6, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 18 }, { "id": "p3.2.20", "order": 22, "type": "table_cell", "bbox": { "l": 117.84, "t": 456.35568, "r": 282.954118, "b": 433.03488 }, "text": "9a Gas Chromatography (and MS) of FAMES", "attrs": { "row": 6, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 19 }, { "id": "p3.2.21", "order": 23, "type": "table_cell", "bbox": { "l": 342.8398, "t": 455.75568, "r": 544.228501, "b": 404.47488 }, "text": "• Transesterification of unknown fat\\n• Apply GC-MS analysis technique used in food industry\\n• ID the fat based on GC-MS data", "attrs": { "row": 6, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 20 }, { "id": "p3.2.22", "order": 24, "type": "table_cell", "bbox": { "l": 41.6398, "t": 400.53504, "r": 47.23708, "b": 390.55488 }, "text": "8", "attrs": { "row": 7, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 21 }, { "id": "p3.2.23", "order": 25, "type": "table_cell", "bbox": { "l": 117.84, "t": 400.53504, "r": 231.714977, "b": 390.55488 }, "text": "Wk 7/8 Capstone Project", "attrs": { "row": 7, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 22 }, { "id": "p3.2.24", "order": 26, "type": "table_cell", "bbox": { "l": 342.8398, "t": 399.93504, "r": 442.775596, "b": 375.91488 }, "text": "• Run reactions\\n• Characterize products", "attrs": { "row": 7, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 23 }, { "id": "p3.2.25", "order": 27, "type": "table_cell", "bbox": { "l": 41.6398, "t": 371.87568, "r": 47.23708, "b": 361.99488 }, "text": "9", "attrs": { "row": 8, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 24 }, { "id": "p3.2.26", "order": 28, "type": "table_cell", "bbox": { "l": 117.84, "t": 341.03908, "r": 212.89928, "b": 331.15828 }, "text": "7b Grignard reaction", "attrs": { "row": 8, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 25 }, { "id": "p3.2.27", "order": 29, "type": "table_cell", "bbox": { "l": 342.8398, "t": 371.37504, "r": 530.168823, "b": 306.55488 }, "text": "• Final characterization if needed\\n• Make and handle water sensitive reaction mixtures\\n• Use acid/base extraction in work up\\n• Recrystallization", "attrs": { "row": 8, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 26 }, { "id": "p3.2.28", "order": 30, "type": "table_cell", "bbox": { "l": 41.6398, "t": 302.61504, "r": 52.87852, "b": 278.11487999999997 }, "text": "10\n11", "attrs": { "row": 9, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 27 }, { "id": "p3.2.29", "order": 31, "type": "table_cell", "bbox": { "l": 117.84, "t": 302.61504, "r": 237.230373, "b": 278.11487999999997 }, "text": "Wk 9/10 Capstone Project\n9b Aldol Condensation", "attrs": { "row": 9, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 28 }, { "id": "p3.2.30", "order": 32, "type": "table_cell", "bbox": { "l": 342.8398, "t": 302.01504, "r": 512.423725, "b": 263.47488 }, "text": "• Class presentation (15 min each)\n• Perform free radical polymerization\\n• Perform condensation polymerization", "attrs": { "row": 9, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 29 }, { "id": "p3.2.31", "order": 33, "type": "table_cell", "bbox": { "l": 41.6398, "t": 259.43568000000005, "r": 52.87852, "b": 249.55488000000003 }, "text": "12", "attrs": { "row": 10, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 30 }, { "id": "p3.2.32", "order": 34, "type": "table_cell", "bbox": { "l": 117.84, "t": 259.43568000000005, "r": 204.38755, "b": 249.55488000000003 }, "text": "12b Polymerization", "attrs": { "row": 10, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 31 }, { "id": "p3.2.33", "order": 35, "type": "table_cell", "bbox": { "l": 342.8398, "t": 258.83568, "r": 488.856672, "b": 234.91488000000004 }, "text": "• Choose recrystallization solvents\\n• ID product by IR and NMR", "attrs": { "row": 10, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 32 }, { "id": "p3.2.34", "order": 36, "type": "table_cell", "bbox": { "l": 41.6398, "t": 230.87568, "r": 52.87852, "b": 220.99487999999997 }, "text": "13", "attrs": { "row": 11, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 33 }, { "id": "p3.2.35", "order": 37, "type": "table_cell", "bbox": { "l": 117.84, "t": 230.87568, "r": 227.393375, "b": 220.99487999999997 }, "text": "10b Multistep Synthesis", "attrs": { "row": 11, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 34 }, { "id": "p3.2.36", "order": 38, "type": "table_cell", "bbox": { "l": 342.8398, "t": 230.39567999999997, "r": 536.370874, "b": 206.47487999999998 }, "text": "• Synthesis of tetraphenylcyclopentadienone\\n• Perform 3 synthesis steps in sequence", "attrs": { "row": 11, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true }, "reading_order": 35 }, { "id": "p3.2.37", "order": 39, "type": "table_cell", "bbox": { "l": 41.6398, "t": 202.53503999999998, "r": 52.87852, "b": 178.03488000000004 }, "text": "14\n15", "attrs": { "row": 12, "col": 0, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 36 }, { "id": "p3.2.38", "order": 40, "type": "table_cell", "bbox": { "l": 117.84, "t": 202.53503999999998, "r": 285.57064, "b": 178.03488000000004 }, "text": "Lab Practical\nFinal Exam Part 2 ACS National Exam", "attrs": { "row": 12, "col": 1, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 37 }, { "id": "p3.2.39", "order": 41, "type": "table_cell", "bbox": { "l": 342.84003, "t": 201.83568000000002, "r": 444.354126, "b": 177.43488000000002 }, "text": "• Covers all experiments\n• Covers all chapters", "attrs": { "row": 12, "col": 2, "rowspan": 1, "colspan": 1, "bbox_refit": true, "merged_continuation": true }, "reading_order": 38 } ], "reading_order": 1 }, { "id": "p3.3", "order": 42, "type": "footer", "bbox": { "l": 34.32, "t": 61.92, "r": 86.64, "b": 49.2 }, "text": "Page 3 of 3", "attrs": { "block_label": "number" }, "reading_order": 2 }, { "id": "p3.4", "order": 43, "type": "footer", "bbox": { "l": 502.08, "t": 60.72, "r": 553.68, "b": 50.16 }, "text": "Rev. 05/2025", "attrs": { "block_label": "footer" }, "reading_order": 3 } ] } ] }