Organic Chemistry Flashcards

1
Q

General Formula

A

The simplest algebraic equation of a homologous series

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Structural formula

A

The minimal detail that shows the arrangement of atoms in a molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Displayed formula

A

The relative positioning of atoms and the bonds between them

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Skeletal formula

A

The simplified organic formula, shown by removing hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Homologous series

A

A series of organic compounds having the same functional group but with each successive member differing CH2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Functional group

A

A group of atoms responsible for the characteristics reactions of a compound

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Aliphatic

A

A compound containing carbon and hydrogen joined together in a straight chains, branched chains or non-aromatic rings

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Alicyclic

A

An aliphatic compound arranged in non-aromatic rings with or without side chains

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Aromatic

A

A compound containing a benzene ring

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Saturated

A

Single carbon-carbon bonds only

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Unsaturated

A

The presence of multiple carbon-carbon bonds, including C=C, C=-C and aromatic rings

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Structural isomers

A

Compounds with the same molecular formula but different structural formulae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Homolytic fission

A

In terms of each bonding atom receiving one electron from the bonded pair, forming two radicals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Heterolytic fission

A

In terms of one bonding atom receiving both electrons from the bonded pair

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Radical

A

A species with an unpaired electron

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Curly arrow

A

The movement of an electron pair, showing either heterolytic fission or formation of a covalent bond

17
Q

Stereoisomer

A

Compounds with the same structural formula but with a different arrangement in 3-D space

18
Q

E/Z isomerism

A

Free rotation is restricted around the double bond so the side with the highest priority can be chosen on a side

19
Q

Cis-Trans Isomerism

A

When the groups on either side are the same

20
Q

Catalyst for Alkenes addition with hydrogen

A

Nickel

21
Q

How to form alcohols from alkene

A

Phosphoric Acid and steam

22
Q

Electrophile

A

Attracted to negatively charged things

An electron pair acceptor

23
Q

Why are alcohols soluble

A

The OH group makes the molecule polar meaning it is attracted to the polar water molecules. Furthermore the OH group can hydrogen bond with the wtpater making it extra soluble

24
Q

Oxidising agent for oxidation of alcohols

A

Cr2O7 2- /H+

K2Cr2O7/ H2SO4

25
Q

Oxidation of primary alcohols under distillation

A

Aldehyde

26
Q

Oxidation of secondary alcohol under reflux

A

Ketone

27
Q

Oxidation of primary alcohol under reflux

A

Carboxylic Acid

28
Q

Nucleophile

A

An electron pair donor