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Addition Reactions of Alkenes

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Total cards: 9•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

What are the reagents of Markovnikov hydrohalogenation reactions?

Back (Answer)

HX

#2
Front (Question)

What are the reagents of Anti-Markovnikov hydrohalogenation reactions?

Back (Answer)

ROOR (alkyl peroxides)

#3
Front (Question)

What does a hydrohalogenation reaction add?

Back (Answer)

Adds a halogen across a pi bond

#4
Front (Question)

Describe the mechanism of a hydrohalogenation reaction.

Back (Answer)

First, there’a a proton transfer. H ends up on the less substituted side, forming a carbocation intermediate and an ion. Then, the ion functions as a nucleophile and attacks the carbocation intermediate.

Card back image
#5
Front (Question)

What is the intermediate of a hydrohalogenation reaction?

Back (Answer)

a carbocation`

#6
Front (Question)

During hydrohalogenation reactions, chiral centers often form. When that happens, what kinds of enantiomers are made?

Back (Answer)

a racemic mixture - equal amounts of both

#7
Front (Question)

What is hydration?

Back (Answer)

the process of adding water (H and OH) across a pi bond

#8
Front (Question)

What is the reaction mechanism for acid-catalyzed hydration?

Back (Answer)

Markovnikov addition. Start with a proton transfer onto the alkene, forming a carbocation intermediate. Next, water functions as a nucleophile and attacks the carbocation, forming an oxonium ion. Finally, water functions as a base and deprotonates the oxonium ion.

Card back image
#9
Front (Question)

What is the reagent for an acid-catalyzed hydration reaction?

Back (Answer)

H3O+ Could also be written as H2O and an acid with brackets around, indicating it’s a catalyst.