Question

Out of (CH3)3C-Br and (CH3)3C-I which is more reactive towards SN1 and why​

Answer 1

A(CH3)3C−I is more reactive towards SN1 than (CH3)3C−Br as I− is a better leaving group than Br

E

Answer 2

The (CH3)3C-I is more reactive towards SN1 reaction than (CH3)3C-Br.

• The stability of the carbocation intermediate created during an SN1 reaction affects the reaction's rate. The SN1 reaction will proceed more quickly the more stable the intermediate carbocation is. Because the bond between carbon and iodine in this case is weaker than the bond between carbon and bromine in (CH3)3C-Br, the (CH3)3C-I substrate is more reactive towards the SN1 reaction.

• The degree to which a chemical species or substance will undergo a chemical reaction or transformation is measured by its reactivity. The type of reactants, the concentration and temperature of the reaction environment, and the presence of catalysts or inhibitors are a few of the variables that affect it.

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