och 4-11

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Last updated 7:52 PM on 7/1/26
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19 Terms

1
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Alkene general molecular formula

CnH2n-2

2
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How are alkynes prepared

Germinal/vicinal dihalides get 2 HX removed by base

3
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What bases can deprotonste an alkyne

NH2 and H-

4
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<p>What mechanism</p>

What mechanism

Hydrohalogenation

5
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Which is slower? Addition of HX to alkenes or alkynes

Alkynes

6
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Name the mechanism

Halogenation

7
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Hydration of alkyne reagents

H2O

H2SO4 and HgSO4

8
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What type of alkyne does a hydration rxn to form a ketone

Internal

9
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What type of alkyne does a hydration rxn to form a methylketone

Terminal

10
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<p>What tautomer form is this</p>

What tautomer form is this

Enol

11
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<p>What tautomer form is this</p>

What tautomer form is this

Keto

12
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<p>What mechanism is this </p>

What mechanism is this

Tautomerization

13
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<p>What mechanism is this </p>

What mechanism is this

Hydration

14
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What is the product of a hydroboration oxi reaction of an internal alkyne

Ketone

15
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What is the product of a hydroboration oxi reaction of a terminal alkyne

Aldehyde

16
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Example bases for terminal alkynes into acetylide ions

NaNH2 and NaH

17
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<p>When an acetylide ion is present…</p>

When an acetylide ion is present…

Undergo Sn2 wedge dash swap

18
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What reaction do 2/3 prime acetylide ions undergo

Elimination via E2

19
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<p>What type of reaction is this</p>

What type of reaction is this

Acetylide Sn2 epoxide opening