Organic Chemistry - Standalone book
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
Question
Book Icon
Chapter 9, Problem 35P
Interpretation Introduction

Interpretation:

The compounds is to be chosen out of the given compounds for the synthesis of 4-methyl-2-pentyne and the synthesis is to be shown.

Concept Introduction:

Alkynes can be prepared by alkylation of acetylene.

Acetylene forms its conjugate base in presence of a strong base like sodium amide.

Reaction of this acetylide anion with alkyl halides produces higher alkynes.

If the alkyl halides are secondary or tertiary, instead of substitution, elimination reaction takes place.

Double dehydrohalogenation of either vicinal or geminaldihalides also produces alkynes.

This reaction occurs in the presence of excess sodium amide.

Blurred answer
Students have asked these similar questions
A. B. b. Now consider the two bicyclic molecules A. and B. Note that A. is a dianion and B. is a neutral molecule. One of these molecules is a highly reactive compound first characterized in frozen noble gas matrices, that self-reacts rapidly at temperatures above liquid nitrogen temperature. The other compound was isolated at room temperature in the early 1960s, and is a stable ligand used in organometallic chemistry. Which molecule is the more stable molecule, and why?
Where are the chiral centers in this molecule? Also is this compound meso yes or no?
PLEASE HELP! URGENT!

Chapter 9 Solutions

Organic Chemistry - Standalone book

Knowledge Booster
Background pattern image
Similar questions
Recommended textbooks for you
Text book image
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Brooks Cole