Topic 17,18 - Organic Flashcards

(38 cards)

1
Q

Chiral centre

A

Carbon with four different substituents; asymmetrical.

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2
Q

Chirality

A

Property of a molecule being non-superimposable on its mirror image.

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3
Q

Plane-polarised light

A

Light oscillating in only one plane.

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4
Q

Polarimeter

A

Device measuring rotation of plane-polarised light.

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5
Q

Enantiomers

A

Optical isomers that are non-superimposable mirror images.

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6
Q

Optical activity

A

Ability to rotate plane-polarised light.

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7
Q

Racemic mixture

A

Equimolar mixture of enantiomers with no net optical activity.

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8
Q

Dimer

A

Molecule of two identical monomers.

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9
Q

Esterification

A

Reaction of alcohol and acid to form ester and water.

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10
Q

Condensation polymerisation

A

Formation of polymers with elimination of small molecules.

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11
Q

Saponification

A

Soap-making by hydrolysis of triglycerides.

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12
Q

SN1

A

Unimolecular nucleophilic substitution with a carbocation intermediate.

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13
Q

SN2

A

Bimolecular nucleophilic substitution with simultaneous bond breaking/forming.

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14
Q

Nucleophilic addition

A

Addition of a nucleophile to a polar double bond.

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15
Q

Tollens’ test

A

Silver mirror test for aldehydes.

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16
Q

Fehling’s and Benedict’s tests

A

Copper-based test for aldehydes (red precipitate).

17
Q

Brady’s reagent

A

2,4-DNPH used to detect carbonyl compounds.

18
Q

Iodoform reaction

A

Identifies methyl ketones or specific alcohols by yellow precipitate.

19
Q

Aromatic

A

Hydrocarbon ring with delocalised π electrons.

20
Q

Kekule model

A

Benzene with alternating single and double bonds.

21
Q

Delocalised model

A

π-electrons delocalised above and below benzene ring.

22
Q

Delocalisation energy

A

Stabilisation due to delocalised electrons in benzene.

23
Q

Halogen carrier

A

Lewis acid catalyst for electrophilic substitution in aromatics.

24
Q

Amines

A

Ammonia derivatives with one or more hydrogens replaced by carbon groups.

25
Basicity
Ability to donate a lone pair to a proton.
26
Amino acids
Organic molecules with -COOH and -NH2 groups.
27
Zwitterion
Molecule with both positive and negative charges, net charge zero.
28
Amphoteric
Ability to react as both acid and base.
29
Isoelectric point
pH at which an amino acid exists as a zwitterion.
30
Amide
Carboxylic acid derivative with -NH2 or similar group.
31
Peptide bond
Covalent bond linking amino acids.
32
Grignard reagent
Organometallic compound used to form carbon-carbon bonds.
33
Hazard
Potential to cause harm.
34
Risk
Likelihood of harm occurring.
35
Reflux
Heating method allowing boiling without loss of solvent.
36
Anti-bumping granules
Prevent vigorous boiling by promoting smooth bubble formation.
37
Miscible
Liquids that mix completely.
38
Recrystallisation
Purification method based on differential solubility.