Final exam

Question 1

Answer 1

Question 2

Answer 2

Question 3

Answer 3

Question 4

Answer 4

Question 5

Answer 5

Question 6

Question 7

Ignoring stereoisomers, how many distinct monochlorinated products form during radical chlorination of the alkanes below?

Answer 7

Question 8

Answer 8

Question 9

Answer 9

There is alkyl halide group here

Question 10

Rank the indicated carbon-carbon bonds in order of increasing bond length (shortest to longest)…

Answer 10

Question 11

Question 12

Answer 12

Question 13

functional groups?

Answer 13

There are alkene alcohol and ester

Question 14

Answer 14

Question 15

Which compound’s pi system resides at a higher energy
in a ground state?

Answer 15

ACETYLENE

Question 16

increasing acidity

Answer 16

Question 17

Answer 17

The lone pair of nitrogen (A) delocalizes around the five membered ring and thus resides in a p-orbital. The lone pair of nitrogen (B)
resides in an Sp2 hybrid orbital and is more readily shared. Nitrogen B is a stronger bronsted base than nitrogen A.

Question 18

Answer 18

Question 19

Answer 19

Question 20

Answer 20

Question 21

Question 22

Question 23

Question 24

Number of asymmetric center and number of stereocenter?

Answer 24

Question 25

Answer 25

Question 26

Answer 26

Question 27

Answer 27

Question 28

Answer 28

Question 29

Answer 29

Question 30

Which of the following reagents will yield a single meso product when reacted with the alkene below? Select all that apply.

Answer 30

no O3

Question 31

Answer 31

Question 32

Answer 32

Question 33

Answer 33

miss the stereochem for methyl shift

Question 34

Answer 34

Question 35

react with H2O, H2So4

Answer 35

Question 36

Answer 36

flip 2 times. got wrong for answer A

Question 37

Answer 37