The reaction of 1-bromohexane with aqueous Na | vedclass

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(C) The reaction of $1$-bromohexane with aqueous $NaOH$ is a nucleophilic substitution reaction. Since $1$-bromohexane is a primary alkyl halide,the r

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second order kinetics

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(C) The reaction of $1$-bromohexane with aqueous $NaOH$ is a nucleophilic substitution reaction. Since $1$-bromohexane is a primary alkyl halide,the reaction proceeds via the $S_N2$ mechanism. In an $S_N2$ mechanism,the rate of reaction depends on the concentration of both the substrate ($1$-bromohexane) and the nucleophile $(OH^-)$. Therefore,the rate law is $Rate = k[CH_3(CH_2)_5Br][OH^-]$. This indicates that the reaction follows second order kinetics.

The reaction of $1$-bromohexane with aqueous $NaOH$ solution follows the order

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