naming rules

Question 1

Parent examples

Answer 1

Phenol, aniline, etc

Question 2

Naming formula

Answer 2

Parent, subs, number subs

Question 3

Cyclohexene plus Br2

Answer 3

Anti addn

Question 4

Benzene plus Br2

Answer 4

No rxn bc benzene is aromatic

Question 5

How to do a frost circle

Answer 5

1. Draw a circle
2. Draw polygon inside it
3. Line for each corner
4. Dotted line in middle
5. Fill in e-

If paired and below center line- aromatic. If above- antiaromatic (very unstable)

Question 6

If a compound doesn’t have a flat ring with overlapping p orbitals, it is

Answer 6

nonaromatic

Question 7

if a compound has a flat ring with overlapping p orbitals but doesn’t have 4N+2 pi electrons, it is

Answer 7

Antiaromatic

Question 8

A lone pair in a P orbital counts as

Answer 8

pi electrons

Question 9

Benzylic position

Answer 9

Directly connected to benzene ring

Question 10

NaCr2O7, H2SO4

Answer 10

Strong oxidizing agent (Alkane chain to CO2H)

Question 11

H2O, Heat

Answer 11

SN1 Substitution reaction with OH

Question 12

NaOH

Answer 12

SN2 substitution with OH

Question 13

Concentrated H2SO4

Answer 13

E1 elimination

Question 14

NaOH

Answer 14

E2 elimination

Question 15

3H2, Ni, high pressure and temp

Answer 15

Turns benzene to cyclohexane

Question 16

H2, Pt, low pressure and temp

Answer 16

Removes DB from vincyclic position

Question 17

Birch reduction

Answer 17

Na, MeOH, NH3- removes DB

Question 18

Birch mechanism (page 12)

Question 19

If EWG present with birch

Answer 19

Pi bonds paralell to group

Question 20

If EDG present with birch

Answer 20

Pi bonds intersect with group