Complete the mechanism and the products for the reaction of 2-pentene with N-bromosuccinimide (NBS) in light and carbon tetrachloride. Use curved arrows, bonds, atoms, and electrons to complete the mechanism and product(s). The first two steps are completed.

Products obtained during this reaction is 1 - bromo - 2 - pentene (Minor)  and 3 - bromo - 2-pentene (Major)

Explanation:

This is the free radical mechanism . Product stability depends on stability of the reaction intermediate obtained during the reaction.

Free radical stability depends on no. of alpha hydrogens.

No. of alpha hydrogen directly proportional with no. of hyperconjugation structure.

hi,

the capital city of australia is canberra.

a: 45.9 meters

b: 4.29 seconds

step-by-step explanation:

a: h(t)=1/2(-9.8)(3)^2+0(3)+90

h(t)=-4.9(3)^2+90

h(t)=-44.1+90

h(t)=45.9 meters

b: 0=1/2(-9.8)(t^2)+0t+90

0=-4.9t^2+90

-90=-4.9t^2

18.37=t^2

t=4.29 seconds

in the second question, the numbers aren't exact, but they're a close approximation.