OWLv2 for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th Edition, [Instant Access], 1 term (6 months)
OWLv2 for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th Edition, [Instant Access], 1 term (6 months)
8th Edition
ISBN: 9781305271593
Author: David W. Oxtoby; H. Pat Gillis; Laurie J. Butler
Publisher: Cengage Learning US
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Chapter 7, Problem 38AP
Interpretation Introduction

Interpretation: All the structural formulas of compound with molecular formula C4H11N needs to be determined if no H atom is directly attached to the N atom.

Concept Introduction: For a molecule, all the structural formulas have same molecular formula but the arrangement of atoms in the molecule is different.

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Feedback (4/10) 30% Retry Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the reactant and missing intermediates involved in this reaction. Include all lone pairs and charges as appropriate. Ignore inorganic byproducts. Incorrect, 6 attempts remaining :0: Draw the Reactant H H3CO H- HIO: Ö-CH3 CH3OH2* protonation H. a H (+) H Ο CH3OH2 O: H3C protonation CH3OH deprotonation > CH3OH nucleophilic addition H. HO 0:0 Draw Intermediate a X
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1. Identify the following alkenes as E or Z NH₂ Br 2. Draw the structures based on the IUPAC names (3R,4R)-3-bromo-4-fluoro- 1-hexene (Z)-4-bromo-2-iodo-3-ethyl- 3-heptene تر 3. For the following, predict all possible elimination product(s) and circle the major product. HO H₂SO4 Heat 80 F4 OH H2SO4 Heat 어요 F5 F6 1 A DII 4 F7 F8 F9 % & 5 6 7 * ∞ 8 BAB 3 E R T Y U 9 F D G H J K O A F11 F10

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OWLv2 for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th Edition, [Instant Access], 1 term (6 months)

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