HNO, H,SO, KMno, H (b) 1. Fe, HCI 2. NaOH NaNO, HCI (4) HO, heat (e) (a) CHOH, H mehybaraben

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 17E
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CHs
OMe
но
methylparaben
(a)
HNO, H,S0.
KMno, H
NANO, HCI
HO, heat
(e)
CH,OH, H
1. Fe, HCI
(c)
methybaraben
2. NaOH
Work out the details of the above retrosynthesis on a separate sheet of paper, and then draw the structure of (e).
• You do not have to consider stereochemistry.
• You do not have to explicitly draw H atoms.
• Do not include lone pairs in your answer. They will not be considered in the grading
• Include counterions for diazonium salts
Transcribed Image Text:CHs OMe но methylparaben (a) HNO, H,S0. KMno, H NANO, HCI HO, heat (e) CH,OH, H 1. Fe, HCI (c) methybaraben 2. NaOH Work out the details of the above retrosynthesis on a separate sheet of paper, and then draw the structure of (e). • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading • Include counterions for diazonium salts
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