Og Flashcards

(46 cards)

1
Q

What is the functional group of an alkene?

A

C=C

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2
Q

What is the functional group of a halogenoalkane?

A

C–Cl, C–Br, C–I

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3
Q

What is the functional group of an alcohol?

A

–OH

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4
Q

What is the functional group of an aldehyde?

A

–CHO

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5
Q

What is the functional group of a ketone?

A

C=O (within chain)

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6
Q

What is the functional group of a carboxylic acid?

A

–COOH

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7
Q

What is the functional group of an ester?

A

–COO–

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8
Q

What is the functional group of an acyl chloride?

A

–COCl

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9
Q

What is the functional group of an amine?

A

–NH₂

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10
Q

What is the functional group of an amide?

A

–CONH₂ (or –CONHR / –CONR₂)

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11
Q

What is the functional group of a nitrile?

A

–C≡N

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12
Q

What is the functional group of benzene?

A

Aromatic ring

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13
Q

What is the functional group of nitrobenzene?

A

–NO₂ on benzene

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14
Q

Alkane → Halogenoalkane (conditions + mechanism)?

A

Free radical substitution; UV light + Cl₂/Br₂

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15
Q

Alkane → Alkene (how?)

A

Cracking using zeolite at ~450°C

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16
Q

Alkene → Halogenoalkane

A

Electrophilic addition with HBr/Br₂

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17
Q

Alkene → Alcohol

A

Hydration with steam + H₃PO₄/H₂SO₄ catalyst

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18
Q

Alkene → Alkane

A

Hydrogenation: H₂, Ni catalyst, 150°C

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19
Q

Halogenoalkane → Alcohol

A

Nucleophilic substitution with aqueous KOH

20
Q

Halogenoalkane → Alkene

A

Elimination using ethanolic KOH + heat

21
Q

Halogenoalkane → Nitrile

A

Nucleophilic substitution, KCN in ethanol, reflux

22
Q

Halogenoalkane → Amine

A

Nucleophilic substitution with NH₃ (ethanolic), heat, excess NH₃

23
Q

Alcohol → Alkene

A

Dehydration using H₂SO₄ + heat

24
Q

Primary alcohol → Aldehyde

A

Oxidation, distil with K₂Cr₂O₇/H₂SO₄

25
Primary alcohol → Carboxylic acid
Oxidation, reflux with K₂Cr₂O₇/H₂SO₄
26
Secondary alcohol → Ketone
Oxidation, reflux with K₂Cr₂O₇/H₂SO₄
27
Alcohol + Carboxylic acid → Ester
Esterification using conc. H₂SO₄
28
Aldehyde → Alcohol
Reduction using NaBH₄ Nucleophilic addition
29
Ketone → Alcohol
Reduction using NaBH₄
30
Aldehyde/Ketone → Hydroxynitrile
Nucleophilic addition with HCN or NaCN + H₂SO₄
31
Carboxylic acid → Ester
Alcohol + conc. H₂SO₄
32
Ester → Alcohol + Carboxylic acid
Acid hydrolysis (H⁺/H₂O)
33
Ester → Alcohol + Carboxylate salt
Alkaline hydrolysis (NaOH)
34
Acyl chloride → Amide
NH₃ (addition–elimination)
35
Acyl chloride → Ester
Alcohol (addition–elimination)
36
Acyl chloride → Carboxylic acid
Hydrolysis with water
37
Nitrile → Amine
Reduction: LiAlH₄ in ether OR H₂/Ni
38
Nitrile → Carboxylic acid
Hydrolysis (H⁺/H₂O or NaOH)
39
Benzene → Nitrobenzene
Electrophilic substitution: conc. HNO₃ + conc. H₂SO₄
40
Nitrobenzene → Phenylamine
Reduction: Sn/HCl under reflux, then NaOH
41
Phenylamine → N-substituted amide
Reaction with acyl chloride
42
Benzene → Aryl ketone
Friedel–Crafts acylation: acyl chloride + AlCl₃
43
Convert alkene → nitrile
Alkene → Halogenoalkane → Nitrile
44
Convert alcohol → amine
Alcohol → Halogenoalkane → Amine
45
Convert carboxylic acid → amide
Carboxylic acid → Acyl chloride → Amide
46
Why can't ketones be oxidised further?
No C–H bond on carbonyl carbon