AS Organic Chemistry Key Terms and Processes Flashcards

1
Q

Why does carbon form a large number of compounds?

A
  • Each carbon atom can form four covalent bonds to other atoms
  • They can be either single, double or triple bonds
  • Carbon atoms can also bond to other carbon atoms forming long carbon chains
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2
Q

Define the term ‘hydrocarbon’

A

A hydrocarbon is a compound containing hydrogen and carbon atoms only

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3
Q

Define the term ‘saturated hydroacrbon’

A

A saturated hydrocarbon has single bonds only

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4
Q

Define the term ‘unsaturated hydrocarbon’

A

An unsaturated hydrocarbon contains carbon to carbon multiple bonds

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5
Q

Define the term ‘Homologous series’

A

A family of hydrocarbons with similar chemical properties who share the same general formula and have the same functional group and each successive member differs by CH2

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6
Q

Define the term ‘functional group’

A

The part of the organic compound that is largely responsible for the molecule’s chemical properties

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7
Q

Define the term ‘aliphatic’

A

Carbon atoms are joined in un-branched or branched chains, or non-aromatic rings

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8
Q

Define the term ‘alicyclic’

A

Carbon atoms are joined to each other in ring structures, with or without branches

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9
Q

Define the term ‘aromatic’

A

Some or all the Carbon atoms are found in a benzene ring

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10
Q

Define the term ‘alkanes’

A

Containing C-C bonds

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11
Q

Define the term ‘alkenes’

A

Containing C=C bonds

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12
Q

Define the term ‘alkynes’

A

Containing at least one triple C to C bond

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13
Q

Define the term ‘empirical formula’

A

Simplest whole number ratio of the atoms of each element present in a compound

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14
Q

Define the term ‘molecular formula’

A

The number and type of atoms of each element present in a molecule

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15
Q

Define the term ‘general formula’

A

the simplest algebraic formula for any member of a homologous series

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16
Q

Define the term ‘displayed formula’

A

Shows the relative positioning of all the atoms in a molecule and the bonds between them

17
Q

Define the term ‘structural formula’

A

Uses the smallest amount of detail necessary to show the arrangement pf atoms in a molecule

18
Q

Define the term ‘skeletal formula’

A

a simplified organic formula that removes:
- all the the carbon and hydrogen labels from carbon chains
- any bonds to hydrogen
And leaves just a carbon skeleton and any functional groups

19
Q

Define the term ‘structural isomerism’

A

Compounds with the same molecular formula nut different structural formulae

20
Q

Covalent bond

A

A shared pair of electrons between two atoms

21
Q

Homolytic Bond Fission

A

When a covalent bond is broken, each of the bonded atoms takes one of the shared pair of electrons from the bond, each atom has a single unpaired electron called a radical

22
Q

Heterolytic Bond Fission

A

When a covalent bond beaks, one of the bonded atoms takes both bonded electrons; the atom that tales both electrons becomes an anion, and the other becomes a cation

23
Q

What do ‘curly arrows’ in reaction mechanisms represent?

A

Used to show the movement of electron pairs when bonds are broken/made

24
Q

Bonding in alkanes

A
  • Each carbon atom is joined to four other atoms by single covalent bonds, sigma bonds, as a result of the direct overlap of two orbitals
25
Q

Shape of alkanes

A

Each C12 atom is surrounded by four e- pairs in four σ bonds, electron pair repulsion results in a tetrahedral structure, with a bond angle of 109.5 degrees

26
Q

Physical Properties of alkanes

A
  • Alkanes have low melting or boiling points because of the very weak intermolecular forces between alkane molecules
  • MP and BP increase with increasing chain length as there are more electrons in molecules, so more London forces
  • insoluble in water, non-polar molecules, no points of attack for polar molecules
27
Q

Chemical properties of alkanes

A
  • generally unreactive, harsh conditions needed to bring about a reaction
28
Q

Physical properties of alkenes

A
  • MP and BP increase with increasing chain length and molecular weight
  • MP and BP lower that respective alkanes, as they cannot pack together as well as alkanes, so less id:id forces are established, hence less energy is required
  • insoluble in water
29
Q

Stereoisomers

A

compounds with the same structural formula but different spatial arrangement

30
Q

E/Z isomers

A

Restricted rotation about the C=C bond, and two different groups should be attached to each of the carbons in the double bond

31
Q

Cis-trans isomers

A

a special case where two groups attached to each C atom of the C=C bond are the same