Rejected
at 4:53 p.m. Feb, 19, 2025 ]
by
pkaps01
Author:
pkaps01
Type of change:
Updated content
Rationale for change
Equation is a huge pain to interpret. Without the inclusion of the chain it makes very little sense. Just moved the image from the extra section.
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1 step
If you were to do an SN1 reaction on a primary substrate, you'd get a primary carbocation, which is very unstable.
| Substrate | polar aprotic solvent | polar protic solvent | strong small base | strong bulk base |
Methyl![]() | SN2 | SN2 | SN2 | SN2 |
Primary![]() | SN2 | SN2 | SN2 | E2 |
Secondary![]() | SN2 | SN1/E1 | E2 | E2 |
Tertiary![]() | SN1/E1 | SN1/E1 | E2 | E2 |
Lecture Notes
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Additional Resources

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