Major Ideas: Alcohols Flashcards

0
Q

Aldehyde

  • functional group
  • suffix/naming
  • main INTERmolecular forces
  • solubility
  • boiling points
A
  • R-CHO
  • ‘al’
  • dipole-dipole forces
  • slightly soluble
  • higher than hydrocarbon, lower than alcohol
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1
Q

Alcohols

  • functional group
  • suffix/naming
  • main INTERmolecular forces
  • solubility
  • boiling points
A
  • R-OH
  • -ol
  • hydrogen bonding
  • soluble in water
  • relatively high
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2
Q

Ketone

  • functional group
  • suffix/naming
  • main INTERmolecular forces
  • solubility
  • boiling points
A
  • R-CO-R
  • ‘one’
  • dipole-dipole
  • slightly soluble
  • similar to aldehyde
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3
Q

Carboxylic acid

  • functional group
  • suffix/naming
  • main INTERmolecular forces
  • solubility
  • boiling point
A
  • R-COOH
  • ‘oic acid’
  • hydrogen bonding
  • soluble in water
  • higher than alcohols
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4
Q

Ester

  • functional group
  • suffix/naming
  • main INTERmolecular forces
  • solubility
  • boiling points
A
  • R-COO-R’
  • alkyl … ‘Oate’
  • dipole-dipole
  • slightly soluble
  • lower than alcohols
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5
Q

Amine

  • functional group
  • suffix/naming
  • main INTERmolecular forces
  • solubility
  • boiling points
A
  • R-NH2
  • ‘amine’
  • hydrogen bonding
  • soluble in water
  • lower than alcohols
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6
Q

Haloalkane

  • functional group
  • suffix/naming
  • main INTERmolecular forces
  • solubility
  • boiling points
A
  • R-X
  • halogen (e.g. Chloro)
  • dispersion and dipole-dipole
  • not in water, but in non-polar solvents
  • low
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7
Q

What is a primary alcohol?

A

One carbon atom and two hydrogen atoms attached to the carbon atom to which -OH group is bonded

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8
Q

What is a secondary alcohol?

A

Two carbon atoms and one hydrogen atom attached to the carbon to which the -OH is bonded (middle)

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9
Q

What is a tertiary alcohol?

A

-OH group bonded to middle carbon along with another functional group

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10
Q

What happens when an alcohol reacts with sodium or potassium?

A

Forms and ask oxide ion and hydrogen gas

- 2ROH + 2Na = H2 + 2RO + 2Na+

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11
Q
What do:
- primary
- secondary 
- tertiary
Alcohols oxidise to?
A
  • primary > aldehyde > carboxylic acid
  • secondary > ketone
  • tertiary doesn’t oxidise
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12
Q

Alcohols and carboxylic acid react to form?

A

Esters

ROH + R’COOH >(H+) R’COOR + H2O

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13
Q

What happens to esters during HYDROLYSIS?

A

Ester bond breaks up

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14
Q

Hydrolysis of esters with acid? (Eqn)

A

R’COOR + H2O = R’COOH + ROH

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15
Q

Hydrolysis of esters with base? (Eqn)

A

R’COOR + H2O = R’COO- + ROH

16
Q

How are alpha amino acids amphorteric?

A

Acid: NH3+ and and COOH
Base: NH2 and COO-
Neutral: NH3+ and COO-

17
Q

What is a zwitterion?

A

Neutral alpha amino acid

- both acidic and basic bond