Synthesis routes for making organic and aromatic compounds

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Alkane -----> Haloalkane
Cl2 and UV light
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Haloalkane ----> Alkene
NaOH, Ethanol and Reflux
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Alkene ----> Haloalkane
HBr, 20 degrees celsius
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Alkene ----> Dibromoalkane
Br2 and 20 degrees celsius
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Alcohol ----> Alkene
Conc. H2SO4 and Reflux
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Alkene ----> Alcohol
H5PO4 catalyst, Steam, 300 degrees celsius and 60 ATM
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Alkene ----> Alcohol
H2O and H2SO4 catalyst
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Haloalkane ----> Alcohol
Warm NaOH and Reflux
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Haloalkane ----> Nitrile
KCN, Ethanol and Reflux
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Nitrile ----> Primary Amine
LiAlH4 and Dilute H2SO4
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Haloalkane ----> Primary Amine
NH3 and Heat
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Haloalkane ----> S/T Amines and Quaternary Ammonium Salts
NH3 and Heat
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Aldehydes/Ketones ----> Alcohol
NaBH4, H2O and Methanol
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Alcohol ----> Aldehydes/Ketones
K2Cr2O7, H2SO4 and heat in a Distillation Apparatus
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Aldehydes/Ketones ----> Hydroxynitrile
KCN or HCN, H2SO4 and 20 degrees celsius
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Aldehydes/Ketones ----> Carboxylic Acid
K2Cr2O7, H2SO4 and Reflux
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Ester ---->Carboxylic Acid
Dilute H2SO4 and Reflux
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Carboxylic Acid ----> Ester
Alcohol, Conc H2SO4 catalyst
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Acyl Chloride ----> Carboxylic Acid
H2O and 20 degrees celsius
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Acyl Chloride ----> Ester
Alcohol and 20 degrees celsius
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Acyl Chloride ----> Primary Amide
NH3 and 20 degrees celsius
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Acyl Chloride ----> N, Substituted Amine
Amine and 20 degrees celsius
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Benzene ----> Nitrobenzene
Conc. H2SO4, Conc. HNO3 and a temperature below 55 degrees celsius
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Nitrobenzene ----> Phenylamine
Sn, Conc. HCL, Reflux and NaOH
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Phenylamine ----> N,Phenylethanamide
CH3COCl
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Benzene ----> Phenylketone
ROCl, AlCl3, Reflux and a non-aqueous environment
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Other cards in this set

Card 2

Front

Haloalkane ----> Alkene

Back

NaOH, Ethanol and Reflux

Card 3

Front

Alkene ----> Haloalkane

Back

Preview of the front of card 3

Card 4

Front

Alkene ----> Dibromoalkane

Back

Preview of the front of card 4

Card 5

Front

Alcohol ----> Alkene

Back

Preview of the front of card 5
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