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Chapter 8.6: Allylic Halogenation

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Total cards: 5•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (5)

#1
Front (Question)

What is a carbon adjacent to a carbon-carbon double bond?

Back (Answer)

allylic carbon

#2
Front (Question)

Describe the mechanism of allylic halogenation

Back (Answer)

o Step 1: Chain Initiation  Chain initiation involves formation of radicals from NBS by light-induced hemolytic cleavage of the N—Br bond in NBS o Step 2: Chain Propagation  Chain propagation involves the formation of products. Reaction of a radical and a nonradical gives a new radical. o Step 3: Chain Termination—The Destruction of Radicals  Propagation if the chain reaction continues until termination steps produce nonradical products and this stop further reaction.

#3
Front (Question)

What is any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon?

Back (Answer)

allylic substitution

#4
Front (Question)

Define allylic substitution

Back (Answer)

any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon

#5
Front (Question)

Define allylic carbon

Back (Answer)

a carbon adjacent to a carbon-carbon double bond