Reason: SN1 occurs in two steps. In the first step, carbocation forms. The rate of reaction in SN1 depends upon the stability of the carbocation, greater the stability faster the reaction. Tertiary (3°) carbocation is more stable than secondary (2°), which is further stable than primary (1°)
By using this
Tert-Butyl Chloride (3°) reacts faster than 3-Chloropentane (2°)
2-Chloro heptane (2°) is more reactive than 1-Chloro hexane (1°)
<p><picture><img src="https://images.shiksha.com/mediadata/images/articles/1690436519phpoW7RUb.jpeg" alt="" width="" height=""></picture></p><p><img src="https://images.shiksha.com/mediadata/images/articles/1690436550phpNyGmAz.jpeg" alt="" width="545" height="81"></p><p>Reason: SN<sub>1</sub> occurs in two steps. In the first step, carbocation forms. The rate of reaction in S<sub>N</sub>1 depends upon the stability of the carbocation, greater the stability faster the reaction. Tertiary (3°) carbocation is more stable than secondary (2°), which is further stable than primary (1°)</p><p>By using this</p><ol><li>Tert-Butyl Chloride (3°) reacts faster than 3-Chloropentane (2°)</li><li>2-Chloro heptane (2°) is more reactive than 1-Chloro hexane (1°)</li></ol>
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