ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL
ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL
8th Edition
ISBN: 9780134595450
Author: Bruice
Publisher: PEARSON
Question
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Chapter 12.5, Problem 8P

(a)

Interpretation Introduction

Interpretation:

For problem 7, the major mono chlorination product obtained on disregarding stereoisomers should be given

Concept introduction:

Distribution of products based on Probability and Reactivity:

Depending on the relative rate of alkyl radical formation, the type of chlorination product obtained differs.  At room temperature, it is 5.00 times easier for a chlorine radical to form a tertiary radical than a primary radical, and it is 3.8 times easier to form a secondary radical than a primary radical.  These, ratios differ at different temperatures

(b)

Interpretation Introduction

Interpretation:

The percentage yield of the major product should be calculated.

Concept introduction:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.

chlorine radical forms a tertiary radical five times faster than a primary radical and it forms a secondary radical 3.8 times faster than a primary radical.

Relative rates of alkyl radical formation by a chlorine radical at 125 °C.

ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL, Chapter 12.5, Problem 8P

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5.Synthesis. Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. Br Br
43. Identify the reagent that will produce the following brominated product in greatest amount. Br A. Br2/uv B. Br2/FeBr3 C. NBS D. B12/CC14 44. Under acidic condition, which of the following compounds can not be oxidized by KMnO4. A. toluene B. 2-butene C. methylcyclohexane D. 2-butyne 45. What alkene product can be produced from the reaction of 2-hexyne with Lindlar's catalyst? A. cis-2-Hexene B. trans-2-Hexene C. Hexane D. A and B
5.Synthesis. Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. Br CH 3 Br CH3

Chapter 12 Solutions

ORGANIC CHEMISTRY-W/S.G+SOLN.MANUAL

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