Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
Related questions
Question

Transcribed Image Text:Give the major organic product of the fol"
through which each reaction proceeds (e.g X
a)
b)
c)
Br
********
www.
OH
********
CH₂
OTS
Br
6M H₂SO4
120°C, distill
reactions. Also, state the mechanism
(Do not draw out the mechanism.)
KOC(CH3)3
in (CH3)3COH
CH₂CH₂CH₂OH
warm
Expert Solution

Step 1
mechanism goes through a carbocation intermediate followed by elimination beta hydrogen that leads to produce alkene product.
Large size base react with alkyl halide through less hindered side of alkyl halide to produce alkene product. This is mechanism.
reaction mechanism involves two steps. First step involves the formation of carbocation and second step involves the nucleophilic attack of nucleophiles leads to produce substituted product.
Step by step
Solved in 2 steps with 1 images
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