Mechanisms Flashcards

1
Q

What does ozonealysis look like and what does it do?

A

Reaction: 1. O3 2. (CH3)S
It cuts double bonds and leaves a double bonded oxygen on both ends of the “cut”

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2
Q

What happens when H2/ (any metal) is reacted with an alkene or alkyne

A

It just “erases” extra bonds and replaces them with a regular single bond

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3
Q

What does an HgSO4, H2SO4, H2O reaction do?

A

All it does is add a double bonded oxygen to the carbon that has priority. (For triple bonds)

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4
Q

What does an (1)(sia)2BH (2)H2O2, NaOH reaction do?

A

All it does is add a double bonded oxygen to the carbon that DOES NOT have priority. (For triple bonds)

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5
Q

What does an Na, NH3 reaction do?

A

It uses one-electron reductions to essential turn triple bonds into double bonds

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6
Q

What does an H2 Lindlar’s catalysts reaction do?

A

It turns a triple bond into a double bond my placing CIS hydrogens on the bond

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7
Q

What does an (1) OsO4, (2) NaHSO3 reaction do?

A

It forms alcohols on both ends of the double bond (turning a alkene into a vicinal diol)

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8
Q

What does an (1) BH3, (2) NaOH, H2O2 reaction do?

A

It adds an OH on the least favored carbon (double bond)

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9
Q

What does an (1) Hg(OAc)2, (2) NaBH4 reaction do?

A

It adds an OH group to the most favorite carbon ignoring re arrangement

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10
Q

What does 2 moles of NaNH2 do?

A

It turns a vicinal dihalide into a triple bond

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11
Q

What does 3 mol NaNH2 do?

A

It turns a vicinal dihalide into a triple bond when it’s on the edge (terminal) (this will result in a lone pair unless there’s is also a H3O step)

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12
Q

What does 1. NaCN 2. H3O+ do to an epoxide?

A

It splits it and adds a CN anti from the OH created

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13
Q

What does PCC do?

A

It takes an alcohol and turns it into an aldehyde (double bonded oxygen and a hydrogen on a carbon)

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14
Q

What are the three ways to make an epoxide from a double bond?

A
  1. (1. Br2 H2O, 2. NaOH)
  2. (RCO3H)
  3. (mcPBA)
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15
Q

What does PBr3 do?

A

It switches out OH with something else (like Br or if there is something else added then whatever that is)

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16
Q

What does H2CrO4 do?

A

It turns an OH into a double bonded O with one mol and with more it can turn a alcohol into a carboxylic acid

17
Q

What does conc. H2SO4 do?

A

It causes an E1 reaction on OH

18
Q

If you have a primary halide what do you have to worry about?

A

Reacting with t-BuOK: E2
Not reacting with t-BuOK: SN2

19
Q

If you have a tertiary halide what do you have to worry about?

A

If you react with a STRONG BASE: E2
If not: SN1/E1

20
Q

If you have a secondary halide what do you have to worry about?

A

If reacting with a strong base: E2
If reacting with a Strong or medium nucleophile: SN2
If a polar proton solvent: Sn1/E1
If not: SN2