Alcohols Flashcards

1
Q

why are alcohols less volatile and have higher melting point than alkanes

A
  • polar -OH on the alcohol can form much stronger H bonds with other -OH groups, on top of the weak London forces present in alkanes
  • more energy needed to overcome these bonds
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2
Q

why are alcohols more soluble in water than alkanes

A
  • the polar -OH group of alcohol molecules, not present in alkanes, can H bond with water
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3
Q

what makes the -OH group polar

A
  • electronegativity of O allows it to attract bonding electrons more than H, giving the H a slightly +ve charge
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4
Q

why does solubility of alcohols decrease with increase in size

A
  • in larger alcohols, most of the molecule is a non-polar C chain so there’s less attraction for the polar H2O molecules
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5
Q

what kind of combustion do alcohols undergo and what does it form

A
  • complete combustion
  • exothermic reaction
  • produces water and carbon dioxide
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6
Q

what reagents is used to oxidise alcohols

A
  • K2Cr2O7/ H2SO4
  • Cr2O7^2-/ H+
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7
Q

Which type of alcohols can’t be oxidised and what would be the observation

A

3*
- solution remains orange

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8
Q

reaction conditions, general equation and observation of oxidation of 1* alcohol to aldehyde

A
  • dilute acid, gentle heating, distillation
  • 1* alcohol + [O] –(CrO7^2-/ H+)–> aldehyde + water
  • colour change from orange to green
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9
Q

reaction conditions, general equation and observation of oxidation of 1* alcohol to carboxylic acid

A
  • conc acid, vigorous heating, reflux
  • 1* alcohol + 2[O] –(CrO7^2-/ H+)–> carboxylic acid + water
  • colour change from orange to green
  • ONLY OXIDATION THAT NEEDS 2[O]
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10
Q

reaction conditions, general equation and observation of oxidation of 2* alcohol to ketone

A
  • conc acid, vigorous heating, reflux
  • 2* alcohol + [O] –(CrO7^2-/ H+)–> ketone + water
  • colour change from orange to green
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11
Q

reaction conditions, general equation and observation of oxidation of aldehydes to carboxylic acids

A
  • dilute acid, vigorous heating, reflux
  • aldehyde + [O] –(CrO7^2-/ H+)–> carboxylic acid
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12
Q

what are elimination reactions

A

when molecule loses atoms, forming a C=C

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13
Q

general equation for the elimination of alcohols to form alkenes

A

alcohol –(conc H2SO4 and heat under reflux)–> alkene + H2O
- there are often 2 possible alkene products from one elimination reaction depending on which side of the -OH group the H is eliminated from
- E/Z isomerism may arise from this

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14
Q

elimination of alcohols to form alkenes is also an example of which type of reaction

A

dehydration

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15
Q

general formula for alcohols

A

CnH(2n+2)O

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