Alkene Reactions Flashcards

1
Q
A

Hydrohalogenation

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2
Q
A

Hydrohalogenation (withRearrangement)

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3
Q
A

Halogenation

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4
Q
A

Hydrobromination with Peroxide

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5
Q
A

Hydration

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6
Q
A

Hydration (with Rearrangement)

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7
Q
A

Bromination in H2O

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8
Q
A

Oxymercuration Demercuration

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9
Q
A

Hydroboration Oxidation

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10
Q
A

Syn-Dihydroxylation

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11
Q
A

Syn-Dihydroxylation

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12
Q
A

Anti-Dihydroxylation

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13
Q
A

Addition of an Alcohol

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14
Q
A

Bromination in Alcohol

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15
Q
A

Catalytic Hydrogenation

Pt can also be used

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16
Q
A

An alkene is treated with HBr (in the absence of
peroxides), so we expect a Markovnikov addition of H and Br across the π bond. That is, Br is installed at the more substituted position:

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17
Q
A

An alkene is treated with HBr in the presence of
peroxides, so we expect an anti-Markovnikov addition ofH and Br across the  bond. That is, Br is installed at the
less substituted position

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18
Q
A
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19
Q
A
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20
Q
A

An alkene is treated with HI, so we expect a
Markovnikov addition of H and I across the  bond. That is, iodine is installed at the more substituted position

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21
Q
A

An alkene is treated with HBr in the presence of
peroxides, so we expect an anti-Markovnikov addition of H and Br across the π bond. That is, Br is installed at the less substituted position

26
Q

Compound A has the molecular formula C5H10. Hydro boration-oxidation of compound A produces 2-methylbutan-1-ol. Draw the structure of compound A.