CNCT ORG CHEM 6 2020
CNCT ORG CHEM 6 2020
6th Edition
ISBN: 9781266807244
Author: SMITH
Publisher: MCG
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Chapter 8, Problem 37P
Interpretation Introduction

(a)

Interpretation: The major stereoisomer formed when the given alkyl halide is treated with KOC(CH3)3 is to be stated.

Concept introduction: In an elimination reaction, the major stereoisomer formed in the one which is most stable. In general, trans isomer is more stable than cis isomer as the substituents are attached far apart from each other causing less steric hindrance.

Interpretation Introduction

(b)

Interpretation: The major stereoisomer formed when the given alkyl halide is treated with KOC(CH3)3 is to be stated.

Concept introduction: In an elimination reaction, the major stereoisomer formed in the one which is most stable. In general, trans isomer is more stable than cis isomer as the substituents are attached far apart from each other causing less steric hindrance.

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Naming the Alkanes a) Write the IUPAC nomenclature of the compound below b) Draw 4-isopropyl-2,4,5-trimethylheptane, identify the primary, secondary, tertiary, and quaternary carbons. c) Rank pentane, neopentane and isopentane for boiling point. pentane: H3C-CH2-CH2-CH2-CH3 neopentane: CH3 H3C-Ċ-CH3 I CH3 isopentane: CH3 H3C-CH2-CH-CH3
Which will evaporate faster, 1-Butanol or Pentane? Explain your choice.
Using the equation below, what is the rate of this reaction if the rate of disappearance of H2 is 0.44 M/sec? H2 + Br2 → 2HBr

Chapter 8 Solutions

CNCT ORG CHEM 6 2020

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