SN2 reaction: Difference between revisions
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trying to recover the model file |
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== S<sub>N</sub>2-Substitution of chloride and methanol == | == S<sub>N</sub>2-Substitution of chloride and methanol == | ||
<Structure size='400' frame='true' align='right' caption='' scene='54/542286/Side_view/ | <Structure size='400' frame='true' align='right' caption='' scene='54/542286/Side_view/2' /> | ||
Typically, alkanes with a substituent in primary position undergo S<sub>N</sub>2 reactions. In contrast to a S<sub>N</sub>1 reaction, no stable carbo cation can be formed. Therefore, another way will be taken. | Typically, alkanes with a substituent in primary position undergo S<sub>N</sub>2 reactions. In contrast to a S<sub>N</sub>1 reaction, no stable carbo cation can be formed. Therefore, another way will be taken. | ||
