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Allylic substitution reactions allow for the attachment of a halogen atom to an alkene without breaking the double bond. Specifically, the halogen attaches to the carbon atom adjacent to the double bonded carbons. This reaction involves heating the alkene with a dihalogen gas like bromine at a high temperature of 500 degrees Celsius, or using N-bromo succinimide or sulfuryl chloride as reactants.
Allylic substitution reactions allow for the attachment of a halogen atom to an alkene without breaking the double bond. Specifically, the halogen attaches to the carbon atom adjacent to the double bonded carbons. This reaction involves heating the alkene with a dihalogen gas like bromine at a high temperature of 500 degrees Celsius, or using N-bromo succinimide or sulfuryl chloride as reactants.
Allylic substitution reactions allow for the attachment of a halogen atom to an alkene without breaking the double bond. Specifically, the halogen attaches to the carbon atom adjacent to the double bonded carbons. This reaction involves heating the alkene with a dihalogen gas like bromine at a high temperature of 500 degrees Celsius, or using N-bromo succinimide or sulfuryl chloride as reactants.
The halogen atom gets attached to the hydrocarbon without breaking the double bond The halogen atom gets attached to the carbon next to double bonded carbon
For Allylic substitution reaction, the alkene is heated with dihalogen gas at high temperature such as 500 celsius or heated with N-bromo succinimide {NBS} or sulphuryl chloride {SO2Cl2}