Module 2 Flashcards

1
Q

Isomers

A

Organic molecules with the same molecular formula but different structural formulae.

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2
Q

Chain isomer

A

Same molecular formula, but different types of chain

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3
Q

Positional isomer

A

Same molecular formula, but different positions of the:
side chain,
substituents or
functional groups on a parent chain

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4
Q

Functional isomer

A

Same molecular formula, but different functional groups

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5
Q

London Dispersion forces

A

weakest

Momentary dipole forms during a collision

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6
Q

Dipole-dipole forces

A

polar molecule

Electrostatic attraction between opposite ends of two molecules

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7
Q

Hydrogen bonds

A

Directional,
strongest,
dipole-dipole bond
H bonded to O, N, F

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8
Q

Covalent bonds

A

Form by overlapping orbitals and shared electron pairs

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9
Q

IMFs

A

The accumulated electrostatic attraction between the molecules

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10
Q

Summarise the general relationship between the length of carbon chain and boiling point of the compound

A

As molecular mass increase,
The strength of the IMFs increases,
The amount of energy needed to separate molecules increases

So boiling point is higher

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11
Q

Vapour pressure

A

The pressure exerted by the evaporated liquid in a closed container.

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12
Q

Why are volatile organic compounds a safety hazard?

A

If compound is flammable and volatile then more molecules are in gas phases and mixed with oxygen in the air and so can ignite/burn/explode.

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13
Q

Equation for the combustion of alkanes

use of alkanes as fuels

A

Alkane + excess oxygen -> carbon dioxide + water

OR

if not enough oxygen is present, incomplete combustion can occur, resulting in formation of CO

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14
Q

Acid catalyst

A

The presence of an acid is used to speed up the reaction

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15
Q

Condensation reaction

A

One of the products is water

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16
Q

Substitution reactions

A

Occur when an atom(s) in an organic molecule is replaced by another atom

17
Q

Addition reactions

A

Where one or more atoms are added across a double bond in a molecule.

18
Q

Name the test we use to test for a carbon-carbon double bond

A

Halogenation

19
Q

Markowikov’s rule

Addition of HX to unsymmetrical alkenes:

A

Hydrogen atom adds to carbon atom already carrying the GREATER number of hydrogen atoms

20
Q

Cracking

A

Breaking long chain alkanes into shorter alkanes and alkenes