all organic reactions Flashcards

1
Q

COMPLETE COMBUSTION alkane + O2 (excess)

A

H20 + CO2

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2
Q

INCOMPLETE COMBUSTION alkane + O2 (not excess)

A

H20 + CO

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3
Q

catalytic converter

A

2CO + 2NO => 2CO2 + N2
2CO + O2 => 2CO2

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4
Q

FREE RADICAL SUBSTITUTION (alkanes)

A

alkane + X2 => haloalkane + HCl
(UV light/sunlight)

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5
Q

CRACKING

A

alkane => alkene + smaller alkane
(Al2O3, heat)

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6
Q

ADDITION
alkene + H2

A

alkane
(Pt/Ni catalyst, heat)

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7
Q

ADDITION
alkene + HX

A

haloalkane
(room temp)

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8
Q

ADDITION
alkene + H2O(g)

A

alcohol
(H3PO4 catalyst, high temp and pressure)

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9
Q

ADDITION
alkene + X2

A

1,2 - dihaloalkane OR 2,2 - dihaloalkane

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10
Q

ALKENE OXIDATION
alkene + [O] + H2O

A

alkane - x,y - diol
(cold, dilute acidified KMnO4)

0 alkyl groups:
CO2 + H2O
1 alkyl groups:
aldehyde
carboxylic acid
2 alkyl groups:
ketone
(hot, concentrated acidified KMnO4)

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11
Q

ALCOHOL SUBSTITUTION
alcohol + HX

A

haloalkane + H2O
(or KX + H3PO4/H2SO4 to make HX)

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12
Q

ALCOHOL SUBSTITUTION
alcohol + PCl3

A

haloalkane + H3PO4
(heat)

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13
Q

ALCOHOL SUBSTITUTION
alcohol + PCl5

A

haloalkane + HCl + POCl3
(rtp)

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14
Q

ALCOHOL SUBSTITUTION
alcohol + SOCl2

A

haloalkane + HCl + SO2
(rtp)

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15
Q

NUCLEOPHILIC SUBSTITUTION
haloalkane + NaOH(aq)

A

alcohol + NaX

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16
Q

HYDROLYISIS
haloalkane + H2O

A

alcohol + HX

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17
Q

NUCLEOPHILIC SUBSTITUTION
haloalkane + KCN

A

alkanenitrile + KX
(ethanolic KCN, heat under reflux)

18
Q

NUCLEOPHILIC SUBSTITUTION
haloalkane + NH3

A

alkylamine + HX

19
Q

ELIMINATION
haloalkane + NaOH(ethanol)

A

alkene + H2O + NaX
(ethanolic NaOH, heat)

20
Q

DISSOLVING ALCOHOLS IN WATER

A

alcohol <=> alkoxide- ion + H+ ion

21
Q

REDUCTION
aldehyde + [H]

A

alco-1-hol
(NaBH4/LiAlH4 red. agent)

22
Q

REDUCTION
ketone + [H]

A

alco-2-hol
(NaBH4/LiAlH4 red. agent)

23
Q

REDUCTION
carboxylic acid + [H]

A

alcohol + H2O
(NaBH4/LiAlH4 red. agent OR H2(g)/ Ni and heat)

24
Q

HYDROLYSIS
ester + dilute acid

A

alcohol + carboxylic acid

25
Q

HYDROLYSIS
ester + alkali (NaOH)

A

alcohol + ethoxide-Na+

26
Q

COMPLETE COMBUSTION
alcohol + O2

A

CO2 + H2O

27
Q

SUBSTITUTION
alcohol + HX

A

haloalkane + H2O
(HCl for this made in situ with NaCl + conc. H2SO4)
(HBr for this made with KBr + conc. H3PO4)

28
Q

alcohol + Na

A

sodium alkoxide + H2

29
Q

ESTERIFICATION

A

carboxylic acid + alcohol <=> ester + H2O
(strong acid catalyst)

30
Q

ESTER HYDROLYSIS
ester + acid/base

A

alcohol + Na alkanoate (or carbox. acid)
(heat under reflux with acid/base)

31
Q

DEHYDRATION
alcohol

A

alkene + H2O
(Al2O3 catalyst, heat

32
Q

OXIDATION
alco-1-hol + [O]

A

aldehyde + H2O
(K2Cr2O7 acidified with dilute H2SO4, heat, orange–green)

33
Q

OXIDATION
alco-2-hol + [O]

A

ketone
(K2Cr2O7 acidified with dilute H2SO4, orange–green)

34
Q

HYDROLYSIS
alkanenitrile + HCl + H2O

A

carboxylic acid + NH4X

35
Q

REDUCTION
carboxylic + [H]

A

alcohol + H2O
(LiAlH4)

36
Q

REDUCTION
aldehyde + [H]

A

primary alcohol
(heat, aq. alkaline NaBH4 OR LiAlH4 in dry ether, rtp)

37
Q

REDUCTION
ketone + [H]

A

secondary alcohol
(heat, aq. alkaline NaBH4 OR LiAlH4 in dry ether, rtp)

38
Q

NUCLEOPHILIC ADDITION
aldehyde/ketone + KCN

A

x - hydroxyalkanenitrile
(heat, catalyst, KCN and dilute H2SO4)

39
Q

TOLLEN’S REAGENT

A

Ag+ + e- => Ag

40
Q

FEHLING’S SOLUTION

A

Cu2+ + e- => Cu+

41
Q

FORMING TRI-IODOMETHANE

A

HALOGENATION
methyl ketone/ethanal +I2 + NaOH(aq) => RCOCI3

HYDROLYSIS
RCOCI3 => RCOO-Na+ + CHI3