Chapter 9 - Properties of Organic Compounds Flashcards

1
Q

Describe dispersion

A
  • non polar regions form instantaneous dipoles.

- weak but accumulative with more electrons

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2
Q

Describe dipole-dipole

A
  • polar molecules form permanent dipoles

- opposing charges on neighbouring molecules are electrostatically attracted to each other.

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3
Q

Describe hydrogen bonding

A

-present when H is bonded to N,O,F. A neighbouring atom must also contain an electronegative element. These are the strongest due to hydrogens little shielding affect and small size.

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4
Q

Describe flashpoint

A

The flashpoint of a volatile liquid is the lowest temperature at which the liquid gives off enough vapour to ignite. weaker intermolecular forces = lower flashpoint as molecule is more volatile

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5
Q

Describe points

A

points refer to melting and boiling point. A high boiling point=strong intermolecular forces. A high melting point=more energy needed to push molecules away from each other.

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6
Q

Describe viscosity

A

-the thickness of a substance (degree of flow)
high viscosity= very thick= no flow
low viscosity= not thick= lots of flow

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7
Q

Hierarchy of hydrogen bonding and functional groups

A
carboxylic acids- QQQQQQQQQQQQQQQQ
alcohols-
amines/amides-
carbonyl/ester- only dipole
basic hydrocarbons- only dispersion
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8
Q

What are structural isomers

A

structural isomers can be

  • chain (different branching)
  • positional (different position of functional group)
  • functional (different functional group but same atoms)
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9
Q

What is Stereoisomerism

A

where molecules are arranged differently around a double or triple bond. Only one common pair has to be used. CIS on the same side TRANS on opposite sides

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10
Q

What is Enantiomerism (optical isomers)

A
  • shown by a chiral centre
  • mirror images are not superimposable
  • carbon is bonded to 4 different molecules
  • bend polarised light in opposing ways
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11
Q

what are the functional isomer pairs?

A

alcohols—-ethers
carboxylic acids—-esters
aldehydes—-ketones

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