Reactions Flashcards

1
Q

alkene to dihaloalkane

mechanism and reactants

A

electrophilic addition

halogen

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2
Q

alkene to haloalkane

mechanism and reactants

A

electrophilic addition

halogen halide

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3
Q

alkene to alkane

mechanism, reactants and conditions

A

electrophilic addition
hydrogen
Nickel catalyst, 150 C , 5 atm
OR Platinum catalyst, room temp and pressure

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4
Q

alkene to alcohol

mechanism, reactants and conditions

A

electrophilic addition
water
c. Sulfuric acid and then dilute with water
OR steam, phosphoric acid catalyst on solid silica, high temp and pressure

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5
Q

haloalkane to alcohol

mechanism, reactants and conditions

A

nucleophilic substitution
ethanolic NaOH OR water
reflux

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6
Q

haloalkane to amine

mechanism, reactants and conditions

A

nucleophilic substitution
ammonia
heat

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7
Q

alcohol to haloalkane

mechanism and reactants

A

nucleophilic substitution

hydrogen halide, strong acid

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8
Q

alkane to haloalkane

mechanism, reactants and conditions

A

radical substitution
halogen
UV light

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9
Q

alcohol to ester

reactants, conditions

A

esterification

carboxylic acid
c.HCl / c.sulfuric acid
reflux

OR acid anhydride
warmed

OR acyl chloride

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10
Q

carboxylic acid to ester

reactants, conditions

A

esterification
alcohol
c.HCl / c.sulfuric acid
reflux

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11
Q

primary alcohol to aldehyde

reactants, conditions

A

oxidation
acidified potassium dichromate (VII)
distilled, excess alcohol

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12
Q

primary alcohol to carboxylic acid

reactants, conditions

A

oxidation
acidified potassium dichromate (VII)
reflux, excess oxidising agent

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13
Q

secondary alcohol to ketone

reactants, conditions

A

oxidation
acidified potassium dichromate (VII)
reflux

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14
Q

alcohol to alkene

conditions

A

dehydration
Alumina catalyst, 300 C
OR c. sulfuric acid catalyst, reflux

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15
Q

Acid hydrolysis of esters

reactants, products, conditions

A

ester + water —–> carboxylic acid + alcohol

dilute acid
excess water to shift equilibrium
reflux

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16
Q

Alkaline hydrolysis of esters

reactants, products, conditions

A

ester + NaOH —-> carboxylate salt + alcohol

reflux

17
Q

Acid hydrolysis of amides

reactants, products, conditions

A

amide + water + HCl —–> carboxylic acid + ammonium/amine salt

heated

18
Q

Alkaline hydrolysis of amides

reactants, products, conditions

A

amide + NaOH —-> carboxylate salt + ammonia/amine

heated

19
Q

ammonia/amine to amide

reactants

A

Acyl chloride

20
Q

Bromination

reactants, products, conditions, mechanism

A

benzene + bromine —> bromobenzene + HBr

FeBr3 (Halogen carrier)
reflux

electrophilic substitution

21
Q

Chlorination

reactants, products, conditions, mechanism

A

benzene + chlorine —> chlorobenzene + HCl

AlCl3 (halogen carrier)
anhydrous

electrophilic substitution

22
Q

Nitration

reactants, products, conditions, mechanism

A

benzene + c.nitric acid (HNO3) + c.H2SO4 —-> nitrobenzene + water
(forms nitrating mixture)

<55 C

electrophilic substitution

23
Q

Sulfonation

reactants, products, conditions, mechanism

A

benzene + sulfuric acid —-> benzenesulfonic acid + H+

reflux

electrophilic substitution

24
Q

Friedel-Crafts alkylation of benzene

reactants, conditions

A

chloroalkane

AlCl3 (halogen carrier)
reflux
anhydrous

25
Friedel-Crafts acylation of benzene | reactants, conditions
acyl chloride AlCl3 (halogen carrier) reflux anhydrous
26
Diazotisation | reactants, products, conditions,procedure
aromatic amine + HNO2 + H+ ----> diazonium ion +2H20 <5 C - amine dissolved in HCl - cold sodium nitrite solution added (forms HNO2) - kept cold in ice bath
27
Coupling reaction | reactants, products, procedure
``` Coupling agent (phenol or aromatic amine) Forms azo dye ``` -coupling agent solution prepared (phenol in sodium hydroxide solution) -Ice-cold diazonium salt solution added
28
Aldehyde with Fehling's solution | what is oxidised/reduced, products, observations
Cu(II) ions reduced to Cu20 Aldehyde oxidised to carboxylic acid Blue solution ----> red precipitate
29
Aldehyde with Tollen's reagent | what is oxidised/reduced, products, observations
Ag+ ions reduced to Ag Aldehyde oxidised to carboxylic acid Silver mirror
30
Aldehyde/ketone to cyanohydrin | mechanism, reactants, conditions
nucleophilic addition HCN acidic conditions