chap 5- whats in a medicine Flashcards

1
Q

what is a primary alcohol

A

an alcohol where the -OH is bonded to a carbon that is bonded to one other carbon atom

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2
Q

what is a secondary alcohol

A

an alcohol where the -OH group is bonded to a carbon that is bonded to 2 other carbon atoms

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3
Q

what is a tertiary alcohol

A

an alcohol where the -OH group is bonded to a carbon that is bonded to 3 other carbon atoms

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4
Q

how are alcohol and water molecules similar

A

both are polar due to the polarised O-H bond. which causes a strong attractive force between molecules

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5
Q

what do the different alcohols produce when oxidised by acidified potassium dichromate

A

primary- aldehydes and then carboxylic acid
secondary- ketones only
tertiary- aren’t oxidised

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6
Q

how do secondary alcohols oxidise to ketones

A

reflux a secondary alcohol with acidified dichromate (VI) to produce a ketone. Ketones can’t be oxidised easily so even prolonged refluxing wont produce anything more

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7
Q

how do you make an alkene from an alcohol

A

eliminate water from the alcohol in a dehydration reaction

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8
Q

what are the 2 methods of dehydrating an alcohol to obtain an alkene

A

1) pass ethanol vapour over a hot catalyst of pumice stone or Al2O3 (catalyst provides large SA)
2) reflux the ethanol with excess conc sulfuric acid at 170c. then collect the ethene produced over water

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9
Q

how can you produce an ester from an alcohol

A

react the alcohol with carboxylic acid or acid anhydrides

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10
Q

alcohol + carboxylic acid=?

A

ester (in the presence of an acid catalyst) usually conc sulfuric or hcl

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11
Q

how can an alcohol be transformed into a haloalkane

A

alcohols react with compounds containing halide ions in a substitution reaction. The -OH is replaced by the halide

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12
Q

what is the formula of phenol

A

C6H5OH

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13
Q

describe the test for phenols

A

add phenol to neutral iron (III) chloride solution and shake, will turn purple

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14
Q

why are phenols described as weak acids

A

they dissolve a little bit in water to form a phenoxide ion and a H+ ion- weakly acidic

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15
Q

what is produced when a phenol reacts with an alkali

A

salt and water

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16
Q

why do phenols not react with carbonate solutions

A

not a strong enough base to remove the hydrogen ion form phenol

17
Q

how can you tell phenols apart from carboxylic acids

A

carboxylic acids react with alkalis and carbonates and give off CO2 gas.
phenols don’t react with carbonates and react with strong alkalis

18
Q

how can you test whether something is a phenol or a different alcohol

A

alcohols and phenols react with acid anhydrides to form an ester and a carboxylic acid.
but phenols will not react with carboxylic acids to form an ester

19
Q

what problem does refluxing avoid

A

organic reactions are slow and substances are flammable and volatile (low bp) so in a beaker they would evaporate or catch fire before they have time to react

20
Q

how do you carry out reflux

A

heat the solution in a flask fitted with a vertical liebig condenser- causes the solution to continuously boil/ evaporate and then condense back into the flask giving it time to react.

21
Q

why should reflux be heated electronically

A

avoids naked flames that could ignite the compoundsq

22
Q

outline the process of distillation

A

heat a mixture in distillation apparatus, substances will evaporate in order of increasing boiling points, evaporated substance enters condenser cools and condenses back into liquid
it can then be collected, themometer shows bp of substance evaporating at any given time