Organic Reactions Flashcards

1
Q

Inductive effect

A

Causes partial charge due to movement of electron cloud, due to difference in electronegativity
+I- positive charge induced
-I: negative charge induced

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Electromeric effect

A

Shifting of pi electrons of a double or triple bond to one of the atoms
+E: electrophile is added
-E: nucleophile is added (electron repulsion, the electrons get added to the atom opposite to the attachment of reagent)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Resonance

A

Movement of Pi electrons along the carbon chain due to addition of FG
+R: groups donate electrons
-R: groups withdraw electons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Hyperconjugation

A

Delocalization of carbon-hydrogen sigma bond.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Reduction of alkene/alkyne to alkane

A

Catalytic hydrogenation: Pd, Raney Ni, Pt in presence of H+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Conversion of alkyl halide to alkane by grignard reagent

A

Formation of R-Mg-X
R-Mg-X+ YZ-H
R-H+ YZ-Mg-X

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Wurtz reaction

A

2(R-X)+ 2Na –dry ether-> R-R 2NaX

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Reduction of alkyl halides

A

R-X –Zn/HCl–> R-H +H-X

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Catalytic Hydrogenolysis

A

R-X +H2 -> R-H + H-X

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Decarboxylation of acids

A

R-COOH + NaOH -> R-COONa+ H2O
R-COONa+ NaOH–CaO-> R-H Na2CO3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Halogenation of alkanes

A

R-H + X –hv–> R-X+ H-X

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Nitration of alkanes

A

R-H + fuming HNO3 –> R-NO2+H2O

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Sulphonation

A

Branched alkanes and higher alkanes form sulphonation in the presence of fuming H2SO4 to form alkanesulphonic acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Formation of methanol

A

2CH4+O2– Cu tube -> 2CH3OH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Formation of methanal

A

CH4+O2– Mo2O3-> HCHO+H2O

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Formation of carboxylic acids

A

R-CH3 + 3O2 –Ag2O-> 2RCOOH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Isomerisation of alkanes

A

Reagent: AlCl3/HCl

18
Q

Aromatization of alkanes

A

Cyclization: Cr2O3, V2O5, Mo2O3/Al2O3
Dehydrogenation

19
Q

Alkynes to alkenes

A

-partial reduction
Lindlar: Pd/CaCO3 and S
Birch: Na/liqNH3

20
Q

Alkyl halides to alkenes

A

Dehydrohalogenation by alc. KOH

21
Q

Saytseff rule

A

The more substituted alkene predominates

22
Q

Alkenes from Vic Dihalides

A

Reagent: Zn+CH3OH

23
Q

Alkenes from gem dihalides

A

Zn dust

24
Q

Acidic dehydration of alkanols

A

Conc. H2SO4 or Al2O3
Forms alkenes

25
Q

Kolbe’s electrolysis

A

R-Na
Or + H2O-> R=R + CO2+H2+KOH
R-K

26
Q

Addition of halogens to alkenes

A

R=R+ X –CCl4–> RX-RX
Test for unsaturation

27
Q

Formation of alkyl halides

A

Trans addition

28
Q

Markovnikov Rule

A

The electronegative atom goes to the carbon atom with less hydrogens

29
Q

Peroxide effect

A

ROOR influences halogen to add to carbon with more hydrogens

30
Q

Addition of hypohalous acids to alkenes

A

Halohydrin is formed; markovnikov addition

31
Q

Indirect hydration of alkenes

A
  1. Formation of isoalkylhydrogensulphate
  2. Undergoes hydration to form alcohols
32
Q

Oxidation of alkenes with oxygen

A

Formation of epoxyalkanes

33
Q

Oxidation of alkenes with potassium permanganate

A
  1. Cold dil (Baeyer’s test)
    Alkylene glycol
  2. Hot KMnO4
    Terminal alkene: carboxylic acid
    Non terminal alkene: Carboxylic acid or ketone
34
Q

Ozonolysis of alkenes

A

Ozonides reduced with Zn dust and water to form aldehyde or ketone

35
Q

Formation of alkyne with calcium carbide

A

CaC2+2H2O-> HC=-CH

36
Q

Formation of alkynes from vic haloalkanes

A

Addition of alc KOH

37
Q

Alkynes from gem dihalides

A

KOH or NaNH2, sodamide in liquid ammonia

38
Q

Formation of alkynes from tetrahalides

A

Heating with Zn and CH3OH

39
Q

Formation of ethyne from haloforms

A

Silver powder

40
Q

Synthesis of higher alkanes from acetylene

A
  1. NaNH2, formation of sodium acetylide
  2. Addition to haloalkane