d. Aflatoxin B, hemiacetal racemizes readily in basic solution.1OCH3H-OHAflatoxin B1 hemiacetale. 4,5-Disubstituted cyclopent-2-enones can rearrange to 2,3-disubstitutedcyclopent-2-enones in basic solution.CH3CH30.5% KOHCH2CH=CHCH½CH3CH2CH=CHCH2CH3

As per the rules, only the first question can be answered. Organic reaction mechanism.

Answered: d. Aflatoxin B, hemiacetal racemizes…

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d. Aflatoxin B, hemiacetal racemizes readily in basic solution. OCH3 O: OH Aflatoxin B1 hemiacetal

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.33P: Two diastereomeric sets of enantiomers, A/B and C/D, exist for 3-bromo-2-butanol. When enantiomer A...

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Concept explainers

Organometallic compounds of d-block elements

The transition metals can form complexes since they have vacant d orbitals. They are also termed Coordination compounds. The organometallic compounds of the transition metals could be used as catalysts as well as reagents. For example, organocadmium, organozinc, organocopper, Grignard are used as the reagents for several reactions. Most of the complexes of organo transition metals are used as catalysts for many organic transformation reactions.

Question

d. Aflatoxin B, hemiacetal racemizes readily in basic solution.
1
OCH3
H-
OH
Aflatoxin B1 hemiacetal
e. 4,5-Disubstituted cyclopent-2-enones can rearrange to 2,3-disubstituted
cyclopent-2-enones in basic solution.
CH3
CH3
0.5% KOH
CH2CH=CHCH½CH3
CH2CH=CHCH2CH3

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