Synthesis Flashcards

1
Q

How do you get from Alkene to Dihaloalkene?

A

X₂
20°C
electrophilic addition

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2
Q

How do you get from Alkene to Alkane?

A

H₂
Ni catalyst
150°C
addition

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3
Q

How do you get from Alkene to Haloalkane?

A

HX
20°C
addition

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4
Q

How do you get from Alkene to Alcohol?

A
H₂O(g) 
conc H₃PO₄ catalyst 
300°C 
60-70atm 
electrophilic addition
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5
Q

How do you get from Alkane to Haloalkane?

A

X₂
UV light
free radical substitution

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6
Q

How do you get from Alcohol to Alkene?

A

conc H₂SO₄
170°C
H.U.R
dehydration/elimination

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7
Q

How do you get from Alcohol to Haloalkane?

A

NaX
H₂SO₄
20°C
nucleophilic substitution

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8
Q

How do you get from Alcohol to Aldehyde/Ketone?

A

H+ K₂Cr₂O₇
H and D/H.U.R
oxidation

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9
Q

How do you get from Alcohol to Ester?

A

carboxylic acid or acyl chloride or acid anhydride
conc H₂SO₄
H.U.R
esterification

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10
Q

How do you get from Aldehyde to Carboxylic Acid?

A

H+/K₂Cr₂O₇
H.U.R
oxidation

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11
Q

How do you get from Haloalkane to Amine?

A

excess ammonia
heat
ethanol

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12
Q

How do you get from Haloalkane to Nitrile?

A

NaCN or KCN
ethanol
H.U.R
H₂SO₄

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13
Q

How do you get from Carboxylic Acid to Ester?

A

alcohol
acid catalyst
heat
esterification

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14
Q

How do you get from Carboxylic Acid to Acyl Chloride?

A

SOCl₂

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15
Q

How do you get from Carboxylic Acid to Alcohol?

A

NaBH₄
H₂O
reduction

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16
Q

How do you get from Ketone to Alcohol?

A

NaBH₄ (aq)

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17
Q

How do you get from Amine to Ammonium Chloride?

A

HCl

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18
Q

How do you get from Alcohol to Carboxylic Acid?

A

H+ K₂Cr₂O₇

H.U.R

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19
Q

How do you get from Carbonyl to Hydroxy Nitrile?

20
Q

How do you get from Nitrile to Amine?

21
Q

How do you get from Carboxylic Acid to Carboxylate Salt?

22
Q

How do you get from Acid Anhydride to Carboxylic Acid?

23
Q

How do you get from Polyamide to Ammonium Salts and Carboxylic Acid?

A

acidic condition

H.U.R

24
Q

How do you get from Polyamide to Amines and Carboxylate Salts?

A

alkaline condition

H.U.R

25
How do you get from Polyester to Alcohols and Carboxylic Acid?
acidic condition | H.U.R
26
How do you get from Polyester to Alcohols and Carboxylate?
alkaline condition | H.U.R
27
How do you get from Acid Anhydride to Ester?
alcohol
28
How do you get from Acid Anhydride to Amide?
NH₃ amine
29
How do you get from Ester to Carboxylic Acid?
dilute HCl NaOH H.U.R hydrolysis
30
How do you get from Aldehyde to Alcohol?
NaBH₄ | reduction
31
How do you get from Ester to Alcohol?
dilute HCl NaOH H.U.R hydrolysis
32
How do you get from Nitrile to Carboxylic Acid?
dilute HCl | H.U.R
33
How do you get from Acyl Chloride to Ester?
alcohol 20°C esterification
34
How do you get from Acyl Chloride to Amide?
``` For primary amide NH₃ 20°C For secondary amide amine 20°C ```
35
How do you get from Acyl Chloride to Carboxylic Acid?
cold H₂O
36
How do you get from Haloalkane to Alcohol?
warm NaOH KOH H₂O H.U.R nucleophilic substitution
37
How do you get from Benzene to Nitrobenzene?
conc HNO₃ conc H₂SO₄ warm
38
How do you get from Benzene to Halobenzene?
X₂ AlCl₃ catalyst warm
39
How do you get from Benzene to Phenyl Ketone?
Acyl chloride AlCl₃ catalyst H.U.R
40
How do you get from Benzene to Alkyl Benzene?
CH₃ AlCl₃ catalyst H.U.R
41
How do you get from Nitrobenzene to Phenylamine?
Tin conc HCl H.U.R then NaOH
42
How do you get from Phenol to 2,4,6 Tribromophenol?
``` bromine water (Br₂) 20°C ```
43
How do you get from Phenol to 2,4 nitrophenol?
dilute HNO₃ | 20°C
44
How do you get from Phenol to Phenyl Ester?
acyl chloride | 20°C
45
How do you get from Phenol to Sodium Phenoxide?
NaOH | 20°C
46
How do you get from Phenol to 2,4,6 Trinitrophenol?
conc HNO₃ | 20°C