Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
Question
Book Icon
Chapter 9, Problem 9.68P
Interpretation Introduction

(a)

Interpretation:

For the given substrate, when NaOH is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when NaOH is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when NaOH is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when NaOH is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when NaOH is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Blurred answer
Students have asked these similar questions
could someone draw curly arrow mechanism for this question please
In the phase diagram of quartz (SiO2), indicate what happens as the pressure increases.
Briefly describe scanning electron microscopy (SEM) and transmission electron microscopy (TEM).

Chapter 9 Solutions

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)

Ch. 9 - Prob. 9.11PCh. 9 - Prob. 9.12PCh. 9 - Prob. 9.13PCh. 9 - Prob. 9.14PCh. 9 - Prob. 9.15PCh. 9 - Prob. 9.16PCh. 9 - Prob. 9.17PCh. 9 - Prob. 9.18PCh. 9 - Prob. 9.19PCh. 9 - Prob. 9.20PCh. 9 - Prob. 9.21PCh. 9 - Prob. 9.22PCh. 9 - Prob. 9.23PCh. 9 - Prob. 9.24PCh. 9 - Prob. 9.25PCh. 9 - Prob. 9.26PCh. 9 - Prob. 9.27PCh. 9 - Prob. 9.28PCh. 9 - Prob. 9.29PCh. 9 - Prob. 9.30PCh. 9 - Prob. 9.31PCh. 9 - Prob. 9.32PCh. 9 - Prob. 9.33PCh. 9 - Prob. 9.34PCh. 9 - Prob. 9.35PCh. 9 - Prob. 9.36PCh. 9 - Prob. 9.37PCh. 9 - Prob. 9.38PCh. 9 - Prob. 9.39PCh. 9 - Prob. 9.40PCh. 9 - Prob. 9.41PCh. 9 - Prob. 9.42PCh. 9 - Prob. 9.43PCh. 9 - Prob. 9.44PCh. 9 - Prob. 9.45PCh. 9 - Prob. 9.46PCh. 9 - Prob. 9.47PCh. 9 - Prob. 9.48PCh. 9 - Prob. 9.49PCh. 9 - Prob. 9.50PCh. 9 - Prob. 9.51PCh. 9 - Prob. 9.52PCh. 9 - Prob. 9.53PCh. 9 - Prob. 9.54PCh. 9 - Prob. 9.55PCh. 9 - Prob. 9.56PCh. 9 - Prob. 9.57PCh. 9 - Prob. 9.58PCh. 9 - Prob. 9.59PCh. 9 - Prob. 9.60PCh. 9 - Prob. 9.61PCh. 9 - Prob. 9.62PCh. 9 - Prob. 9.63PCh. 9 - Prob. 9.64PCh. 9 - Prob. 9.65PCh. 9 - Prob. 9.66PCh. 9 - Prob. 9.67PCh. 9 - Prob. 9.68PCh. 9 - Prob. 9.69PCh. 9 - Prob. 9.70PCh. 9 - Prob. 9.71PCh. 9 - Prob. 9.72PCh. 9 - Prob. 9.73PCh. 9 - Prob. 9.74PCh. 9 - Prob. 9.75PCh. 9 - Prob. 9.76PCh. 9 - Prob. 9.77PCh. 9 - Prob. 9.78PCh. 9 - Prob. 9.79PCh. 9 - Prob. 9.80PCh. 9 - Prob. 9.81PCh. 9 - Prob. 9.82PCh. 9 - Prob. 9.83PCh. 9 - Prob. 9.84PCh. 9 - Prob. 9.1YTCh. 9 - Prob. 9.2YTCh. 9 - Prob. 9.3YTCh. 9 - Prob. 9.4YTCh. 9 - Prob. 9.5YTCh. 9 - Prob. 9.6YTCh. 9 - Prob. 9.7YTCh. 9 - Prob. 9.8YTCh. 9 - Prob. 9.9YTCh. 9 - Prob. 9.10YTCh. 9 - Prob. 9.11YTCh. 9 - Prob. 9.12YTCh. 9 - Prob. 9.13YTCh. 9 - Prob. 9.14YTCh. 9 - Prob. 9.15YT
Knowledge Booster
Background pattern image
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning