Alcohols Flashcards

1
Q

what is the functional group of an alcohol

A

hydroxyl group -OH

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2
Q

what is the general formula of an alcohol

A

CnH2n+1OH

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3
Q

what kind of intermolecular forces do alcohols have and why

A

hydrogen bonding due to the electronegativity difference in the OH bond

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4
Q

how do BP and MP of alcohols compare to other hydrocarbons of the same C length and why

A

higher

they have hydrogen bonding which is stronger than VDW

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5
Q

are alcohols soluble in water and why does solubility depend on chain length

A

soluble when short chain as OH bonds to hydrogen bonds in water

insoluble when long chain as the non polar C-H bonds takes precedence

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6
Q

what makes an alcohol primary

A

C bonded to OH is only bonded to one other C atom

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7
Q

what makes an alcohol secondary

A

when the C that the OH is bonded to is bonded to 2 other C atoms

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8
Q

how can ethanol be made from crude oil

A

hydration of ethene via electrophilic addition

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9
Q

what are the advantages and disadvantages of using electrophillic addition to make crude oil

A

+ fast
+ continuous process

  • not renewable
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10
Q

how can ethanol be made by fermentation

A

plant carbohydrates are broken down and fermented by enzymes in yeast

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11
Q

what conditions are needed for fermentation to make ethanol

A

enzymes in yeast as catalyst

35 degrees

anaerobic conditions

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12
Q

write an equation for fermentation

A

C6H12O6 (aq) —-> 2C2H5OH + 2CO2

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13
Q

what are the advantages and disadvantaged of using fermentation to make ethanol

A

+ renewable as its from plants

  • slow
  • needs to be fractionally distilled
  • batch process
  • enzymes stop working at 15% alcohol
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14
Q

define the meaning of carbon neutral

A

no net addition of CO2 to the atmosphere

carbon dioxide is released when combusted but absorbed by plant

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15
Q

write an equation for the combustion of ethanol

A

C2H5OH + 3O2 —> 2CO2 + 3H2O

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16
Q

what is an elimination reaction

A

the removal of a smaller molecule from a larger one

17
Q

which group leaves the parent molecule in the case of alcohols

A

OH and a H to form water

18
Q

what different physical conditions are needed for the elimination reaction from alcohols to alkenes
(describe 2)

A

excessive hot concentrated sulphuric acid

pass vapour over hot aluminium oxide

19
Q

draw a mechanisms for the dehydration of ethanol

A

refer to word document

20
Q

draw and describe the method for distilling cyclohexanol into cyclohexene

A
  1. concentrated H2SO4 and H3PO4 are added to a round bottom flask containing cyclohexanol and mix the solution by swirling and add bumping granules
  2. connect the flask to distillation apparatus and gently heat to cyclohexene boiling point the mixture using an electrical heater
  3. chemicals with boiling points up to cyclohexene will evaporates and the warm gas rises and condenses
21
Q

what forms if you partially oxidise a primary alcohol

A

an aldehyde

22
Q

what conditions are needed to partially oxidise a primary alcohol

A

dilute sulfuric acid and potassium dichromate

distill product as its produced and gently heat

23
Q

write an equation for the partial oxidation of ethanol

A

CH3CH2OH + [O] —> CH3CHO + H2O

24
Q

what forms is you fully oxidise a primary alcohol

A

a carboxylic acid

25
what conditions are needed for the complete oxidation of a primary alcohol
acidified potassium dichromate reflux and heat strongly
26
write an equation for the full oxidation of ethanol
CH3CH2OH + 2[O] --> CH3COOH + H2O
27
what forms if you oxidise a secondary alcohol
a ketone
28
why cant you oxidise a secondary alcohol any further than a ketone
a carbon carbon bond would have to break
29
what conditions are needed foe the oxidation of a secondary alcohol
acidified potassium dichromate reflux and heat strongly
30
write an equation for the oxidation of propan-2-ol
CH3CH(OH)CH3 + [O] ---> CH3COOH + H2O
31
what is in Tollens reagent and how does this react with the substance to be tested
silver nitrate in NH3 oxidises aldehydes but not ketones complex Ag+ ions reduced to Ag
32
how do you carry out the Tollens test
add equal volumes of substance being tested and tollens reagent to a test tube leave in water bath for 10 minutes and observe chnages
33
what does Fehlings solution give a positive test result for
aldehydes
34
what is in Fehlings solution and how does this react with the substance to be tested
Blue copper (II) complex ions which are gentle oxidising agent reduced to Cu+ ions which are brick red
35
what conditions do you need to use the Fehlings solution
Heat
36
describe the separation of the cyclohexene made in distillation from the mixture
1. product collected after the distillation eill still contain some impurities which need to be removed 2. transfer the product mixture to a separation funnel and add water to dissolve water soluble impurities and create an aqueous solution 3. allow the mixture to settle into layers and drain off the aqueous layer at the top leaving the impure cyclohexene
37
describe the steps of purification of cyclohexene after distillation and seperation
1. drain off the impure cyclohexene into a round bottom flask 2. add anhydrous CaCl2 and a stopper flask and let the mixture dry for 20 minutes with occasional swirling 3. distil mixture one more time