Alkene Reactions #1 - Narrated Answer Key 

Wonderful explanations!

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

This is so helpful. Thank you!

Helped me so much in learning this chapter thank youuu!

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?

Wonderful....... God bless you.....

Helped me in my revision

very informative! thanks!

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 :)

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Nice

Thanks a lot ma'am .

First year thank you

B will be syn or anti addition?

Nice one

Please explain how the structure came about

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

Roci or racimic i can't see d handwriting

For B, wouldn't it also be racemic?

what the fuck?