Reagents & Conditions

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Bromoalkane to primary amine
NH3 (dry, in ethanol, warm)
1 of 19
Alkene to primary alcohol
Conc. H2SO4 (catalyst), reflux, 170 degrees
2 of 19
Alkene to alkane
Steam, 150 degrees, Nickel (catalyst)
3 of 19
Alkene to bromoalkane
HBr, 20 degrees
4 of 19
Bromoalkane to secondary alcohol
NaOH (aq), reflux
5 of 19
Benzene to chlorobenzene
Cl2, halogen carrier (catalyst), warm
6 of 19
Benzene to nitrobenzene
Conc. H2SO4, Conc. HNO3, 50-60 degrees
7 of 19
Nitrobenzene to phenylamine
tin, conc. HCL, reflux, add NaOH (aq)
8 of 19
Phenylamine to Benzene diazonium chloride (diazotisation)
HNO2, HCL, < 10 degrees
9 of 19
Benzene diazonium chloride to azo dye (coupling)
Phenol, NaOH (aq),
10 of 19
Phenol to 2,4,6-tribromophenol
Br2 (aq) , 20 degrees
11 of 19
Phenol to sodium phenoxide
Na metal or NaOH, 20 degrees
12 of 19
Alcohol to aldehyde, carb. acid or ketone
oxidising agent, reflux
13 of 19
Aldehyde, carb. acid or ketone to alcohol
NaBH4, heat
14 of 19
Aldehyde to carb, acid
oxidising agent, reflux
15 of 19
Alkene to dibromoalkane
Br2 (aq), 20 degrees
16 of 19
Alkane to bromoalkane
Br2, UV light
17 of 19
Acid anhydride to ester
Alcohol, warm
18 of 19
Carb. acid to ester
Alcohol, H2SO4, reflux
19 of 19

Other cards in this set

Card 2

Front

Conc. H2SO4 (catalyst), reflux, 170 degrees

Back

Alkene to primary alcohol

Card 3

Front

Steam, 150 degrees, Nickel (catalyst)

Back

Preview of the back of card 3

Card 4

Front

HBr, 20 degrees

Back

Preview of the back of card 4

Card 5

Front

NaOH (aq), reflux

Back

Preview of the back of card 5
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