SN2 reaction: Difference between revisions
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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 load='SN2_animation3d. | <Structure load='SN2_animation3d.xyz' size='400' frame='true' align='right' caption='' scene='' /> | ||
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. | ||
