Chap 18 Flashcards

0
Q

What can be created from 1,3 dithiane ?

A

Keytones and aldehydes

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1
Q

1,3-dithiane is a cyclic ring with what two atoms a the 1 and 3 positions

A

Sulfur

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2
Q

The first step in creating a keytone with 1,3 dithiane is

A

Removing a hydrogen with a strong base

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3
Q

After removing a hydrogen from 1,3 dithiane what must be done to the anion to create a keytone?

A

Alkyl halides are added to mixture so the anions will attack the alkyl group

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4
Q

What reagents must be added to the alkylated dithiane to create a keytone.

A

H+

Mercury dichlorate ( HgCl2)

H2O

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5
Q

What’s the first step in creating a keytone from a Carboxylic acid

A

Removing the hydrogen form the acid and creating a lithium complex in its place.

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6
Q

What compound can be used in the first step to create a keytone from a Carboxylic acid

A

Methyl lithium

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7
Q

The second step of the Carboxylic acid to keytone consists of

A

Adding a alkyl group to to the central carbon with an Organo lithium or grignard.

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8
Q

After adding an alkyl group what must be done to create a germinal diol

A

Addition of the oxygens with acid

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9
Q

The last step of the Carboxylic acid to keytone reaction is

A

The geminal diol reconfiguring to a keytone

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10
Q

What is the first step in creating Keytones from alkyl nitriles

A

Addition of anlkyl group to the 1carbon of the nitrile with a grignard

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11
Q

After adding a grignard to the nitrile what is the last step in creating the keytone

A

Addition of H3O+

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12
Q

What are the reagents for creating a keytone from an alkyl nitrile

A

Grignard reagent
Alkyl nitrile
H3O+

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13
Q

Acid chloride can be reduced to an aldehyde with what long complex reactant

A

Lithium tri-tert- butoxyaluminiumhydride ( Li+ -AlH(O-t-Bu)3 )

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14
Q

Acid chloride can be reduced to a keytone with what

A

Lithium dialkylculprates ( R2 CuLi)

R = any alkyl group.

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15
Q

What is the main point of a witting reaction

A

Converts Keytones and aldehydes to alkenes

16
Q

The witting reaction uses what reactants

A

Keytone or aldehyde

Ylide

17
Q

What is a ylide

A

Tri phenyl phosphorus stabilized Carbanion

18
Q

What is involved in a ylide synthesis

A

Tri phenyl phosphine attacks an alkyl halide to produce a phosphonium salt.

A strong base ( butyl lithium) reacts with the salt to produce the ylide

19
Q

In acid conditions H2O and an aldehyde or keytone create what

A

Keytone hydrate

20
Q

What compound is the hydrate of a keytone

A

Germinal diol

21
Q

A hydrate can be created in basic conditions with

22
Q

What reactants for a cyanohydrin

A

Aldehyde or Keytones

Cynide -CN

23
Q

Imine synthesis is a result of what reagents

A

Keytones or aldehyde

Ammonia( NH3)
Alkyl amine  (R-NH2)
24
Formation of acetals and Keytols requires
2 equivalents of alcohol Keytone or aldehydes H+
25
A ketone and One equivalent of alcohol will produce what
Hemiketol
26
What is the product a diol and an aldehyde
Cyclic acetal
27
Ramey Ni will reduce a Keytones to what
Alcohol
28
Clemmonson reduction requires what reactants
Zn(Hg) HCl H2O
29
What is hydrazine
Carbon double bonded to a nitrogen which is attached to an amine
30
What is the purpose of a wolf kisher reduction.
Fully reduce a Keytone to a methyl
31
Silver oxide. (Ag2O). Is what
Oxidizing agent.
32
Wolff kisher reduction requires how many steps.
2
33
What is the first step of the kisher reduction
Addition of a di amine to a Keytone to produce hydrzone
34
The second step of the kisher reduction is to
Remove the di amine witha strong base
35
What is created after the second step of the kisher reduction
Fully reduced Keytone.
36
Trolleys test looks for what in an unknown mixture
Aldehydes
37
What is used is a tollens test
2 Ag(NH2)2 3 OH-
38
How does the tollens test confirm there is aldehydes
Create a silver mirror effect