Alkenes Flashcards

1
Q

Synthesis of alkenes and R&C

A
  1. Elimination of water from alcohol
    - excess conc H2SO4, 170 degrees
  2. Elimination of HX from halogenoalkanes
    - Ethanolic NaOH
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Electrophilic addition of HX(g)

A
  • HI(g)/HCl(g)/HBr(g), room temp
    to get halogenoalkane
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Electrophilic addition of X2(g)

A
  • Cl2(g)/Br2(g) or Br2 in CCl4
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Electrophilic addition of X2(aq)

A
  • Cl2(aq)/Br2(aq), room temp
    get halohydrin
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Reduction of alkenes

A
  • H2 gas, Ni catalyst, heat
  • get alkane
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Mild Oxidation

A
  • cold KMnO4, H2SO4(aq)
  • get diol
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Strong oxidation

A
  • hot KMnO4, H2SO4(aq)
  • add O to double bond, Oh to replace H
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Racemic mixture

A
  • Carbocation is trigonal planar
  • X- nucleophile can attack carbocation from either sides of the plane with equal probability
  • racemic mixture is formed and is optically inactive
How well did you know this?
1
Not at all
2
3
4
5
Perfectly