Allene's Flashcards

(43 cards)

1
Q

Elimination of water from alcohols

A

Excess conc h2so4 180*
Conc h3PO4, 200-250*
Al2O3, 350*

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2
Q

Electrophilic addition of halogen

A

Br2(l) in CCl4/ Cl2(g) in ccl4

Absence of light, rt

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3
Q

Electrophilic addition of hydrogen halides

Hydrohalogenation

A

HCl, HI, HBr(g)

Room temp

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4
Q

Electrophilic addition of steam

Industrial

A

H2O(g)
H3PO4 as catalyst
300*, 60 atm

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5
Q

Electrophilic add of steam

Laboratory

A

Conc H2SO4 followed by H20(l), warm

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6
Q

Catalytic hydrogenation (addition of hydrogen)

A

H2, finely divided nickel, 200-300*, 4 ATM

Or platinum catalyst or palladium catalyst, rt and pressure

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7
Q

Strong oxidation

A

KMnO4 in dil H2SO4, heat under reflux

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8
Q

Mild oxidation

A

KMnO4 in aq Koh or naoh

Cold

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9
Q

Electrophilic sub of nitration to benzene

A

Conc Hno3 conc H2SO4

Reflux at 55*

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10
Q

Halogen atom (benzene)

A

X2

Fe filings or FeX3 or AlX3

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11
Q

Nitration of methylbenzene

A

Conc HNO3 Conc H2SO4

30*

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12
Q

Halogenation of methylbenzene

A
X2 
Iron filings
FeX3
alX3
In the dark rt
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13
Q

Halogenation of side chain (methylbenzene

A

X2
Presence of Uv light
Heat

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14
Q

Oxidation of methylbenzene

A

Dil H2SO4, KMnO4

Heat under reflux

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15
Q

Formation of alcohol from RX

A

Naoh(aq) or koh(aq)

Heat under reflux

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16
Q

Formation of nitrile from RX

A

Ethanolic or alcoholic NACN (kcn) heat under reflux

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17
Q

RCOOH from RCN

A

Dil H2SO4

Heat under reflux

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18
Q

RCOO- from RCN

A

Aq NAOH

heat under reflux

19
Q

RCN to RCH2NH2

A

LiAl4 in dry ether

H2, nickel, 200-300/platinum and palladium rt

20
Q

RNH2 from RX

A

Excess conc NH3 In ethanol, heat in a sealed tube

21
Q

Elimination of HX From RX to form Allene

A

Ethanolic NAOH or KOH

Heat under reflux

22
Q

Reduction of aldehydes and ketone to alcohol

A

LiAL4, in dry ether
H2, Pt catalyst
Sodium borohydride (NABH4) in ethanol
Na in ethanol

23
Q

Reduction of carboxylic acid to alcohol

A

LialH4 in dry ether

24
Q

Alcohol to alkoxide (RONa)

25
Formation of ester via alcohol with cooh
Carboxylic acid, conc H2SO4(small limited) | Heat under reflux
26
Alcohol and acid chlorides(ClCOR) to form ester
Acid chloride, rt
27
Alcohol with hydrogen halide to form halogen halide
NaBr with conc H2SO4 heat under reflux | ZnCl2 and conc HCl heat under reflux
28
Alcohol with PX3 or PX5
For RI: I2 + phosphorus, heat | PCL3, PCl5, anhydrous, rt
29
Alcohol with thionyl chloride (SOCL2)
SOCL3, anhydrous rt
30
Ethanolic koh(Naoh) heat under reflux
Removal of hydrogen halide
31
Alcohol - tri iodomethane rxn
I2 (aq) with NAOH(aq), warm | Yellow solid of CHI3 formed
32
Phenol with Na
Na metal, rt
33
Phenol with base
NaOH(aq) rt
34
Phenol to ester
Acid chlorides (CH3COCL) , rt
35
Nitration for phenol
Dilute HNO3 Rt concentrated -> trinitrophenol
36
Bromination in phenol
Aq Bromine Rt -> 246-trinitrophenol Br (l) in CCl4 rt
37
Aldehyde and ketone with HCN
HCN | Presence of catalyst (NACN or Kcn, or traces of base such as NAOH)
38
Hydrolysis of Cyanohydrine (-COOH)
H20, dil HCL, heat
39
Reduction of cyanohydrine (-CH2NH2
LiAlH4 in dry ether
40
Oxidation of aldehyde by tollen reagent
``` Complex of (Ag(NO3)2)+ in alkaline sol Silver formed ```
41
Oxidation of aldehyde by fehling sol
Complex of Cu2+ in alkaline sol
42
Aldehyde and ketone with 2-4 dinitrophenylhydrazinr
2,4 DNPH dil H2SO4 as catalyst, warm Yellow or orange crystalline solids
43
Iodofoam reaction with aldehydes and ketones
Iodine in aq NAOH | Warm