# Where should we place alpha,beta unsaturated carbonyls in the reactivity order list?

In this question, reasons for this observed trend of reactivity of different types of carbonyl compounds are discussed.

I would like to know where we can place $\alpha,\beta$ unsaturated carbonyls in this list.

Initially I thought we can place them above acyl chlorides because now we have 2 electrophilic carbons but then I think the reactivity of both of the carbons should also be reduced because of conjugation so they should be placed somewhere in the middle, but where exactly?

• What carbonyls? Ketones? – Mithoron Jul 12 '18 at 19:00
• Both aldehydes and ketones @Mithoron – Archer Jul 12 '18 at 19:09
• Well, they are already there, as ketones and aldehydes. – Mithoron Jul 12 '18 at 19:30
• @Mithoron Presence of adjacent unsaturation is going to affect reactivity, isn't it? – Archer Jul 12 '18 at 19:31
• Everything does, but you seem to overestimate it. – Mithoron Jul 12 '18 at 19:40