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15 Cards in this Set
- Front
- Back
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free radical substitution |
limited halogen, UV light |
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electrophilic addition of alkene (to form alcohol) |
1) steam, high T&P, conc H3PO4 catalyst 2) cold conc H2SO4 followed by hot water |
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electrophilic addition of alkene (to form halogenoalkane) |
1)dry HX 2)HX in CCl4 |
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electrophilic addition of alkene (to form halogenoalkane) |
1)X2 in CCl4 in the dark 2) X2 (gas/liquid) in the dark |
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electrophilic addition of alkene (forming alcohol) |
aqueous X2 |
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Reduction of alkene |
1)H2 gas, Ni catalyst, high temp and pressure 2)H2 gas & Pd/Pt catalyst |
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Mild oxidation of alkene |
cold alkaline KMnO4 |
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Strong oxidation of alkene |
1) hot acidified kmno4 2) hot alkaline kmno4 |
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Nitration of arene (electrophilic addition) |
conc hno3 & conc h2so4 & 55 degree celcius |
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halogenation of arene (electrophilic substitution) |
X2 with anhydrous FeX3/AlX3 or Fe catalyst |
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friedel-craft alkylation of benzene (electrophilic substitution) |
R-X with anhydrous FeX3/AlX3 |
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Nitration of methyl benzene |
conc h2so4 conc hno3, 30 degree celcius |
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halogenation of methyl benzene (electrophilic substitution) |
X2 with anhydrous FeX3/ AlX3 |
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free radical substitution of methyl benzene ( react with side chain alkyl) |
limited X2, UV light |
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side chain oxidation of methyl benzene |
KMnO4 in dilute h2so4, heat |
