Chapter 21 ending portion for exam 3: The chemistry acid derivatives

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Last updated 9:16 PM on 4/24/26
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42 Terms

1
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What nucleophiles do acid chloride’s react with?

1) Ammonia and Amines

2) Alcohols and Phenols

3) Carboxylate Salts

2
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What reagent does a carboxylic acid react with to make an acid chlorides?

SOCl2

or

PCl5

3
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What is made when you react an acid chloride with an amine?

amide

4
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What is made when you react an acid chloride with an alcohol or a phenol?

ester

5
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What is made when you react an acid chloride with a carboxylate?

an anhydride

6
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What is the chemical formula for an acetyl group?

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7
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What is the chemical formula for an ester?

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8
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What is the chemical formula for a pyridine?

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9
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What is the chemical formula for an sufonyl chloride?

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10
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What is the chemical formula for an acid chloride?

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11
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What is the chemical formula for a nitrile?

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12
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What is the chemical formula for an aldehydes?

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13
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What is the chemical formula for an anhydride?

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14
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What is the chemical formula for a carboxylate?

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15
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What is the chemical formula for an amide?

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16
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What is the chemical formula for an ammonia?

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17
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What is the chemical formula for an amine?

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18
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What can form when an anhydride reacts with an amine nucleophile?

amide

19
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What is made when an anhydride reacts with a carboxylic acid nucleophile?

an ester

20
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What is made when a cyclic anhydride reacts with an alcohol nucleophile? What is the base formula?

Half ester formation

<p>Half ester formation</p>
21
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What is made when cyclic anhydride reacts with an amine nucleophile? What is the base formula?

half amide formation

<p>half amide formation</p>
22
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What is made when you react an ester with an amine or ammonia?

amide

23
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What is made when you react an ester with an hydroxylamine? What is the base formula?

Hydroxamic acid

<p>Hydroxamic acid</p>
24
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What is the formula for a hydroxlamine?

NH2OH

25
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What is made when you react an ester with an alcohol?

trans esterification

26
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What happens in transesterification?

switch the oxygens and their R groups of the alcohol and the ester

  • then give the hydrogen of the alcohol to the R group of the oxygen that was initially attached to the ester

27
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What does the reduction of ester make?

primary alcohol

28
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What determines the substitution of alcohols? (ie. primary, secondary, and tertiary)

The number of carbons that are connected to the carbons that is directly connected to the alcohol

29
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What reagent is used for the reduction of ester?

lithium aluminum hydride (LiAlH4)

30
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What does the reduction of Amides make? What reagent is used?

they form primary, secondary, and tertiary amines using the reagent LiAlH4

31
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What does the reduction of nitriles make? What reagents are used?

primary amines

cause use LiAlH4 or Raney Nickel

32
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What determines the substitution of amine? (ie. primary, secondary, and tertiary)

it is determined by the amount of carbons the amine is directly connected to

33
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What does the reduction of acid chlorides make? What reagent is used?

aldehydes and uses LiAlH4 derivatives as reagents

34
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What does the reaction of esters with grognard reagents make?

alcohols

35
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What does the reaction of acid chlorides and Dialkylcuprates make? Why are diallkylcuprates used instead of grignards reagents?

ketone

  • it is easier to control condition to yield a ketone

36
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What is the general name given to a group of polyamides?

nylon

37
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What are polyesters?

they are condensation polymers derived from diols and dicarboxylic acids

38
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What does condensation polymers in the creation of polymers mean?

the OH from the carboxylic acid and an H from the alcohol are taken off and combined to make water (H2O)

39
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What are diols?

a molecule with two alcohols groups

40
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What is a dicarboxylic acid?

a molecule with two carboxylic groups

41
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What is the formula of a ketone?

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42
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