organic info Flashcards

1
Q

When is an amine a nucleophile?

A

When an amine lone pair reacts to form a bond with any atom other than H, we say it is acting as a nucleophile.

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2
Q

When is an amine a base?

A

When an amine lone pair reacts to form a bond with an H+ ion( basically a proton) it is a base

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3
Q

The general formula of cyclic alkenes is?

A

CnH2n-2

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4
Q

draw the mechanism for the reaction of bromoethane with ammonia

A

https://cognitoedu.org/coursesubtopic/c3-alevel-aqa_PwogFJjU

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5
Q

describe this Organic reaction :
Addition

A
  • The joining of two or more molecules to form a larger molecule.
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6
Q

describe this Organic reaction :
Elimination

A
  • An atom or a small group of atoms detaches from a larger molecule.
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7
Q

describe this Organic reaction : Substitution

A
  • One atom or group is replaced by another.
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8
Q

describe this Organic reaction : Hydrolysis

A

Hydrolysis - A molecule splits by incorporating H+ and OH- from water.

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9
Q

describe this Organic reaction :
Oxidation

A
  • A process where a species loses electrons to an oxidising agent, represented by [O] in equations.
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10
Q

describe this Organic reaction :
Reduction

A

Reduction - A process where a species gains electrons from a reducing agent, represented by [H] in equations.

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11
Q

describe this reagent : Nucleophiles

A

Electron pair donors. They contain lone pairs or negative charges and can donate those electrons during reactions since they are electron rich.

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12
Q

Examples of nucleophiles include

A

OH-,CN-,NH3( you only need to know these 3 in AS level according to aqa specification)

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13
Q

describe this reagent : Electrophiles

A

Electrophiles - Electron pair acceptors. They are electron deficient and can accept electron pairs during reactions.

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14
Q

Examples of Electrophiles include

A

Examples include H+ / partially positive , Br partially positive

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15
Q

describe this reagent : radicals

A

Radicals - Species with one (or more) unpaired electrons. Their unpaired electron makes them highly reactive. They do not donate/accept electron pairs but can react with most chemical bonds, including non-polarised C-C and C-H bonds.

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16
Q

Examples of radicals include

A

Examples include Cl* and CH3Cl* radicals.
*= DOT

17
Q

Heating under reflux means…

A

Heating under reflux means heating with a condenser placed vertically in the round bottom flask with heat under it to prevent loss of volatile substances from the mixture
https://study.com/cimages/multimages/16/706a7b11-c558-4f1c-afc7-11e37e7a4d88_figure_11.png

18
Q

Potassium hydroxide and sodium hydroxide are both strong ?, but ? has a slightly higher?.

A

Potassium hydroxide and sodium hydroxide are both strong alkalis, but potassium hydroxide has a slightly higher alkalinity.

19
Q

OH- acts as a ? in elimination reactions by removing a ?.

A

OH- acts as a base in elimination reactions by removing a proton(H+).

20
Q

A base is

A

something that reacts with an acid to form water and a salt.

21
Q

An alkali is

A

any base that is soluble in water.

22
Q

Substitution is favoured in ? solution. OH- acts as a ? here.

A

Substitution is favoured in aqueous solution. OH- acts as a nucleophile here.

23
Q

Elimination is favoured in ? solution. OH- acts as a ? here.

A

Elimination is favoured in ethanolic solution. OH- acts as a base here.

24
Q

how can you get both elimination and substitution reactions to occur?

A

Using a solvent mixture of water and alcohol allows both reactions to occur, giving a mixture of products.

25
how to isolate the aldehyde after oxidation of primary alcohol...
- gently heat the alcohol in a distillation apparatus with a limited amount of potassium dichromate(VI) - then distil the aldehyde as it forms to prevent further oxidation.
26
To obtain the carboxylic acid after oxidation of primary alcohol...
heat the alcohol with an excess of dichromate(VI) under reflux conditions.