organic reactions Flashcards

1
Q

alkane and oxygen reaction

A

excess of oxygen
forms carbon dioxide and water
combustion reaction

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2
Q

alkane and halogen reaction

A

UV light
halogenoalkane formed
free radical substitution

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3
Q

halogenoalkane and sodium hydroxide (aq) reaction

A

heat under reflux
alcohol and halide ion formed
nucleophilic substitution/hydrolysis reaction

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4
Q

halogenoalkane and CN-

A

heat under reflux, ethanolic
halide ion and nitrile formed
nucleophilic substitution

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5
Q

halogenoalkane and ammonia reaction

A

heat, ethanolic
amine and ammonium halide salt formed
nucleophilic substitution

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6
Q

what does heating under reflux ensure

A

no volatile reactants are lost

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7
Q

why are some substitution reactionswith done in ethanolic conditions

A

otherwise an alcohol would form instead of the desired product

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8
Q

how to form an amine from an ammonium salt

A

add sodium hydroxide

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9
Q

halogenoalkane and sodium hydroxide (ethanolic) reaction

A

hot, ethanolic
elimination reaction
alkene forms

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10
Q

which alcohols are more likely to undergo substitution and which are more likely to undergo elimination

A

primary- substitution
tertiary- elimination

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11
Q

do higher temperatures favour elimination or substitution

A

elimination

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12
Q

reaction for depletion of ozone

A

uv light present in upper atmosphere
Cl. +O3 –> ClO. + O2
ClO. + O3 –> Cl. + 2O2

free radical is regenerated
chain reaction

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13
Q

how do chlorine radicals form

A

homolytic fission of chlorine with uv light

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14
Q

alkene and sulfuric acid reaction

A

conc. sulfuric acid
alkyl hydrogen sulfate formed
electrophilic addition

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15
Q

what is formed when alkyl hydrogen sulfate is heated

A

alcohol

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16
Q

what determines which product is formed from unsymmetrical alkenes

A

the stability of the intermediate carbocation

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17
Q

alkene and HBr reaction

A

HBr gas
bromoalkane formed
electrophilic addition

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18
Q

alkene and bromine reaction
uses of this reaction

A

bromine liquid or bromine water
dibromoalkane formed
electrophilic addition
useful to test for alkene

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19
Q

alkene and steam reaction

A

heat and phosphoric acid catalyst
alcohol formed
electrophilic addition/ acid-catalysed hydration

20
Q

what acts as an electrophile in the electrophilic addition reaction of alkene to alcohol

A

H3O+ (formed from water and acid catalyst)

21
Q

fermentation reaction

A

yeast present, warm, anerobic conditions
ethanol and carbon dioxide formed from glucose

22
Q

why is yeast needed and warm, anerobic conditions for glucose fermentation

A

yeast- organism which carries out anerobic respiration of glucose
warm- optimum temperature for enzye action
anerobic- so yeast don’t respire anerobically

23
Q

why does fermentation of glucose stop after a certain point and how can this be prevented

A

yeast are killed
prevented by distilling the ethanol off

24
Q

alcohol and acidified potassium dichromate reaction

A

heat, acid catalyst
primary alcohol -> aldehyde (when distrilled) -> carboxylic acid (under reflux)
secondary alcohol -> ketone
oxidation reaction

25
alcohol and conc. acid catalyst
conc. sulfuric/ phosphoric acid catalyst alkene formed elimination/ dehydration reaction
26
reduction of aldehydes/ketones reaction
NaBH4 reducing agent provides H- ions aldehydes- forms a primary alcohol ketones- forms a secondary alcohol
27
aldehyde/ ketone and KCN reaction
KCN in sulfuric acid forms a hydroxynitrile may form a racemic mixture of 2 entaniomers in equal amounts
28
carboxylic acid plus metal (e.g zinc) reaction
carboxylic acid salt (zinc carboxylate) plus hydrogen formed
29
carboxylic acid and alcohol reaction
heat under reflux, conc. sulfuric acid catalyst ester formed reversible reaction condensation/ esterification reaction
30
why is an acid catalyst needed for esterification reaction
reaction is reversible so acid catalyst pushes eqm right to form more ester
31
ester hydrolysis reaction
warm, aqueous dilute acid or alkali plus ester forms carboxylic acid and alcohol
32
acyl chloride and water reaction
forms carboxylic acid and HCl nucleophilic addition-elimination
33
acyl chloride and alcohol reaction
ester and HCl formed nucleophilic addition-elimination
34
acid anhydride plus water reaction
carboxylic acid formed addition-elimination
35
acid anhydride and alcohol reaction
forms ester and carboxylic acid addition-elimination
36
benzene plus nitric acid reaction
conc. nitric acid and conc. sulfuric acid catalyst forms nitrobenzene electrophilic substitution/ nitration reaction
37
formation of nitronium ion reaction
HNO3 + H2SO4 --> H2NO3+ + HSO4- H2NO3+ --> NO2+ + H2O overall eqn. : HNO3 + 2H2SO4 --> +NO2 + 2HSO4- + H3O+
38
benzene and acyl chloride reaction
warm, AlCl3 catalyst forms aromatic ketone electrophilic substitution/ friedel crafts acylation
39
formation of the acylium ion reaction
RCOCl + AlCl3 --> [RCO]+ + [AlCl4]-
40
nitrile reduction reaction
nitrile reducing agent- LiAlH4 and dry ether catalyst/ hydrogen gas and nickel catalyst forms an amine reduction/ hydrogenation reaction
41
why does dry ether need to be used with LiAlH4
else it reacts violently with water
42
nitroarene reduction reaction
add nitroarene, HCl (and NaOH) Tin (Sn) catalyst aromatic arene formed reduction reaction
43
forming polyester reaction
dicarboxylic acid and diol forms a polyester condensation polymerisation
44
forming polyamide reaction
dicarboxylic acid and diamine forms polyamide condensation polymerisation
45
amino acid condensation reaction
forms a polyamide/ polypeptide
46
removal of sulfur dioxide eqn
SO2 + CaO --> CaSO4
47
lithium half cell eqn.
Li+ + e- ⇌ Li E⦵ = -3.04V CoO2 + Li+ + e- ⇌ LiCoO2 E⦵ = +0.56 V