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There's a question about inhibition of resonance:

Is steric inhibition of resonance or steric inhibition of protonation dominant in o-toluidine?

If you look at Martin's answer he says that CH3 is not bulky enough to cause steric inhibition of resonance. What if I considered a group such as ethyl or propyl or even bulkier, then would we observe SIP (steric inhibition of protonation) as well as steric inhibition of resonance?

What would dominate?

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  • $\begingroup$ You can make a follow-up question if it's significantly different. $\endgroup$ – Mithoron Jul 12 '18 at 19:48

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