The regiochemistry of Electrophilic Addition to Conjugated Dienes HBr faster becasue of the Br proximity + Br Br The Br* is still next of the H 1,2-Adduct major at 0º C Becasue it forms faster H Br Farther apart e Br H 1,4-Adduct major at 40° C Becasue it is more stable

Draw the product of (2Z,4Z)-hexa-2,4-diene and light. Need answer fast i'll rate up

Can this carbocation rearrange to a more stable one?

Mono addition of HBr to unsymmetrical dienes generally produces four products – two 1,2-addition products and two 1,4-addition products. Draw the reactant diene that forms the four products shown, and identify the addition route that forms each product. Select /// Draw Rings C H More Erase Q2 2 Q HBr product 1 product 2 product 3 Br product 4 Br Br Br