Alkene Reactions #1 - Narrated Answer Key

This is a predict-the-product problem set on alkene and alkene reactions (addition and reduction reactions).

[yashdaryani]

for (I), wouldn't you have two compounds since both carbons are secondary carbons and so the bromine could either end up with carbon #3 or carbon #2 since they're equally stable?

[yasmine]

Helped me so much in learning this chapter thank youuu!

[allesklar]

In problem D there is the formation of two tertiary carbocations. However the stabilization is the product of hyperconjugation. The position "1" with the methyl group gets stabilized by 3 C-H-bonds whereas in position "2" with the ethy group it should only get stabilized by 2 C-H-bonds since its -CH2-CH3. So im thinking that the more stable product ist the one wehre the Cl sits on Position "1". Am I thinking about this wrongly? Help or correction would be appreciated, thanks :)

[SS-pnss]

Great video, sums up a lot of ideas, thank u so much <3

[justicegabriel]

Please explain how the structure came about

[irmaanayancyramos]

For B, wouldn't it also be racemic?

[rameshgaurav]

In G 14:10 will there be no formation of hexane ?

[laurenbling]

Roci or racimic i can't see d handwriting