reaction of functional groups Flashcards

1
Q

aldehyde to 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

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8
Q

halogenoalkane to alkene

A

NaOH
ethanol
heat

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9
Q

halogenoalkane to alcohol

A

aqueous NaOH
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

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
heat under reflux

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16
Q

alcohol to aldehyde

A

primary alcohol
acidified K2Cr2O7
distil

17
Q

keytone/aldehyde to alcohol

A

LiAlH4 - source of H- ions
dry ether
hydrolysis

18
Q

gringard reagent to alcohol

A

HCOH
RCHO
RCOR’

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*
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
ester to carboxylic acid
HCL or H2SO4 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
alcohol to ester
NaBH4
33
benzene to
34
alkene to alcohol
steam acid
35
halogenoalkane to esther
alcohol - ethaolic KOH / NaOH carboxylic acid -pottasium dichromate vi -sulfuric acid esther -react alcohol with carboxylic acid -sulphuric acid catalyst
36
diol from phenoalkene
pottasium manganate vii
37
alcohol to carboxylic acid
potassium dichromate vi and dilute sulfuric acid heat under reflux forms water colour change from —- to green
38
cyclicalcohol to cyclicalkene
elimination experiement phosphoric acid heat use distilation and seperating funell then dry
39
Cyclic