Organic Pathways Flashcards

(31 cards)

1
Q

State the reagents and conditions for converting alcohols to esters

A

Carboxylic acid
Conc. H2SO4

Heat reflux

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2
Q

State the reagents and conditions for converting esters to alcohols, what reaction is this?

A

Water, dilute H2SO4

Heat reflux

Hydrolysis

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3
Q

State the reagents and conditions for converting carboxylic acids to esters

A

Alcohol, conc. H2so4

Heat reflux

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4
Q

State the reagents and conditions for converting esters to alcohols, what type of reaction is this?

A

Water
Dilute h2so4

Heat reflux

Hydrolysis

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5
Q

State the reagents and conditions for converting alcohols to aldehydes, what type of reaction is this?

A

Acidified potassium dichromage

Intermediate distillation

Oxidation

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6
Q

State the reagents and conditions for converting secondary alcohols to ketones, what reaction is this?

A

Acidified potassium dichromate
Heat reflux

Oxidation

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7
Q

State the reagents and conditions for converting alcohols to COOH? What type of reaction is this?

A

Acidified potassium dichromate

Heat reflux

Oxidation

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8
Q

State the reagents and conditions for converting ketones/ aldehydes to hydroxynitriles. What reaction is this?

A

KCN and dilute HCl

Dilute acid

Nucleophilic addition

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9
Q

State the reagents and conditions for converting ketones/ aldehydes to alcohols. What reaction is this?

A

NaBH4

Aqueous

Nucleophilic addition

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10
Q

State the reagents and conditions for converting alcohols to alkenes, what reaction is this?

A

Conc. H2so4

Heat

Elimination

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11
Q

State the reagents and conditions for converting alkenes to alcohols, what reaction is this?

A

Steam

Phosphoroc acid, high temp and pressure

Hydration

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12
Q

State the reagents for converting alkenes to halogenoalkanes, what reaction is this?

A

H-X (hydrogen halide)

Electrophilic addition

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13
Q

State the reagents and conditions for converting halogenoalkanes to alkenes? What reaction is this?

A

NaOH

Ethanolic acid
Heat
Aqueous

Elimination

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14
Q

State the reagents for converting acyl chlorides/ acid anhydrides to esters. What reaction is this?

A

Alcohols

Nucleophilic addition elimination

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15
Q

State the reagents for converting acyl chlorides/ acid anhydrides to COOH. What reaction is this?

A

Water

Nucleophilic addition elimination

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16
Q

State the reagents for converting acyl chlorides/ acid anhydrides to primary amides. What reaction is this?

A

Amides

Nucleophilic addition elimination

17
Q

State the reagents and conditions for converting alkanes to halogenoalkanes, what mechanism is this?

A

Halogens

UV light

Free radical substitution

18
Q

State the reagents and conditions for converting alkanes to halogenoalkanes, what mechanism is this?

A

Halogens

UV light

Free radical substitution

19
Q

State the reagents and conditions for converting halogenoalkaes to a nitrile, what mechanism is this?

A

KCN aq

Ethanolic, heat

Nucleophilic substitution

20
Q

State the reagents and conditions for converting halogenoalkanes to primary amines, what mechanism is this?

A

EXCESS ammonia

Heat, aqueous, ethanol

Nucleophilic substitution

21
Q

What are the reagents and conditions for converting a nitrile to amine, and what reaction is this?

A

H2

Nickel catalyst, high temps and high pressure

Reduction

22
Q

What are the reagents and conditions for converting primary amines to secondary amines? What type of reaction is this?

A

Nucleophilic substitution

R-X and excess primary amine
Heat

23
Q

What are the reagents and conditons for converting sedomdary amines to tertiary amines? What mechanism is this?

A

Nucleophilic substitution

R-X, excess secondary amine
Heat

24
Q

What are the reagents for converting primary amines to sedondary amides? What mechanism is this?

A

Nucleophilic addition elimination

Reagents- Acyl chloride

25
What are the reagents and conditions for converting benzene to nitobenzen? What mechanisms is this?
Conc. HNO3 and conc. H2SO4 Reflux 50* Electrophilic substitution
26
What are the reagents and conditions for converting benzene to a phenylketone? What mechanism is this?
Acyl chloride, with anhydrous AlCl3 Electrophilic sub
27
What are the reagents and conditions for converting nitrobenzene to a phenylamine? What reaction is this?
Tin and conc. Hcl Heat reflux Reduction
28
What are the reagents for converting a phenylamine to a N-phenylethanamide? What mechanism is this?
Acyl chloride Nucleophilic addition elimination
29
What are the regents and conditions for converting halogenoalkanes to alcohols? What mechanisms is this?
NaOH aqueous Heat Nucl sub
30
What is organic synthesis?
Using reaction mechanisms to create a target molecule form a starting molecule
31
In organic synthesis, why do you try and keep the number of steps as low as possible?
To improve the percentage yield of the final product