WM1: Development Flashcards

1
Q

Why are alcohols polar molecules?

A

Because of the polarised O-H bond due to electronegativity of Oxygen

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2
Q

Which bond type is stronger; Covalent or Hydrogen bonding?

A

Covalent

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3
Q

Describe the trend in solubility as you increase the length of the carbon chain on an alcohol.

A

Solubility decreases due to the polarity of the O-H bond becoming less important to the molecule compared to the carbon chain.

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4
Q

Give the definition for a primary, secondary, and tertiary alcohol

A
primary = -OH bonded to a carbon bonded to one other carbon atom.
secondary = -OH bonded to a carbon bonded to two other carbon atoms.
tertiary = -OH bonded to a carbon bonded to three other carbon atoms
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5
Q

What colour change would we see when a dichromate ion is used to oxidise an alcohol group

A

orange to green

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6
Q

Give the conditions required to go from ethanol to ethanal

A

Oxidation with potassium dichromate with the alcohol in excess distilled

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7
Q

Give the conditions required to go from ethanol to ethanoic acid

A

Oxidation with potassium dichromate with the Oxidising agent in excess under reflux

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8
Q

When under reflux, what is the maximum height the vapour should condense at in the condenser?

A

halfway up (some liebig condensors have a vapour ring)

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9
Q

What colour would potassium dichromate be when added in excess to 2-methylpropan-2-ol and refluxed

A

Remains orange because 2-methylpropan-2-ol will only oxidise once to form the ketone.

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10
Q

What conditions are required for the dehydration for alcohol to the alkene

A

alumina catalyst at 300 degrees

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11
Q

What conditions are required for the esterification of an alcohol with a carboxylic acid

A

Strong acid catalyst heated under reflux.

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12
Q

Name the following molecule:

CH3COOCH2CH3

A

ethyl ethanoate

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13
Q

Name the following molecule:

CH3CH2OCH2CH2CH3

A

Propyl ethyl ether

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