reaction of functional groups Flashcards

1
Q

aldehyde to carboxylic acid
e,g ethanal to lactic acid
CH3CH(OH)COOH - lactic

A

1
-nucleophillic addition
-HCN + KCN
CH3CHO + HCN –> CH3CH(OH)CN
2
-hydrolysis
-strong acid
-heat under reflux
CH3CH(OH)CN + 2H2O + H+ –> CH3CH(OH)COOH + NH4+

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2
Q

keytone/aldehyde to alcohol

A

LiAlH4
dry ether

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3
Q

carboxylic acid to alcholol

A

LiAlH4
dry ether

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4
Q

alcohol to esther

A

conc H2SO4
esterfacation

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5
Q

alkane to halogenoalkane

A

Cl2 , Br2 ect
UV light
free radical substitudtion

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6
Q

alkene to alkane

A

H2
Nickel catalyst
150*
margarine can be made

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7
Q

alkene to halogenoalkane

A

hydrogen halide
25*

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8
Q

halogenoalkane to alkene

A

NaOH/KOH
warm ethanol
heat under reflux

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9
Q

halogenoalkane to alcohol

A

aqueous NaOH/KOH
heat under reflux

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10
Q

halogenoalkane to amine

A

conc NH3
ethanol
heat under pressure

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11
Q

halogenoalkane to nitrile

A

aq KCN
ethanol
heat under reflux

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12
Q

halogenoalkane to gringard reagent

A

Mg
dry ether

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13
Q

alkene to dihalogenoalkane

A

X2
room temp

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14
Q

alcohol to halogenoalkane

A

conc HX or PCl5
dif method for each halogen

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15
Q

alcohol to keytone

A

secondary alcohol
acidifed K2Cr2O7
H2SO4
heat under reflux

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16
Q

alcohol to aldehyde

A

primary alcohol
acidified K2Cr2O7
H2SO4
distil

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17
Q

keytone/aldehyde to alcohol

A

LiAlH4 - source of H- ions
dry ether
hydrolysis

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18
Q

gringard reagent to alcohol

A

HCOH
RCHO
RCOR’

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19
Q

keytone/aldehyde to hydroxynitrile

A

KCN with HCN

20
Q

carboxylic acid to aldehyde

A

LiAlH4
dry ether
hydrolysis

21
Q

aldehyde to carboxylic acid

A

acidified K2Cr2O7
heat under reflux

22
Q

gringard reagent to carboxylic acid

A

CO2
hydrolysis

23
Q

nitrile to amine

A

H2
nickel catalyst
150* under pressure
LiAlH4
dry ether
hydrolysis

24
Q

nitrile to carboxylic acid

25
carboxylic acid to ester
ROH heat conc H2SO4
26
carboxylic acid to acyl chloride
PCl5 room temp
27
carboxylic acid to esther
react with alcohol sulphuric acid catalyst heat under reflux
28
acyl chloride to ester
ROH room temp
29
acyl chloride to carboxylic acid
H2O room temp
30
acyl chloride to amide
conc NH3
31
amine to secondary amide
acyl chloride room temp
32
esther to an alcohol
NaBH4
33
alkene to alcohol
steam H3PO4 catalyst 300* / 60 atm or H2SO4 catalyst water
34
halogenoalkane to esther
alcohol - aqeous ethaolic KOH / NaOH carboxylic acid -pottasium dichromate vi -sulfuric acid esther -react alcohol with carboxylic acid -sulphuric acid catalyst
35
diol from phenoalkene
pottasium manganate vii
36
alcohol to carboxylic acid
potassium dichromate vi and dilute sulfuric acid heat under reflux forms water colour change from —- to green
37
cyclicalcohol to cyclicalkene
elimination experiement phosphoric acid heat use distilation and seperating funell then dry
38
cyclichexane to cyclichalagenoalkane
halogen uv light free radical substitution
39
cyclichalagenoalkane to cyclicalcohol
aqeous sodium hydroxide
40
cyclicalkene to cyclicalkane
hydrogen platnum catalyst
41
gringards with carbon dioxide
carboxylic acid
42
gringards with methanal
primary alcohol
43
gringards with aldehyde
secondary alcohol
44
gringards with keytone
tertiary alcohol
45
methyl keytone/methyl secondary alcohols with iodine
sodium hydroxide yellow precipitate -triiodomethane (iodoform) and carboxylate salt with one fewer carbon atoms
46
benzene to acetly chloride
use gringards
47
2-bromo-2-methylbutane to 2,2-dimethylbutan-1-ol
2-bromo-2-methylbutane reacts with Mg -Dry ether * CH3CH2C(MgBr)(CH3)CH3 * react Grignard reagent with HCHO *CH3CH2C(CH3)2CH2OMgBr * (hydrolyse) with (dilute) acid