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AQA A-Level Chemistry Organic Synthesis - Statistics
General Stats
- This quiz has been taken 44 times
- The average score is 8 of 89
Answer Stats
| start | end | answer (if empty just put x) | % Correct | |
|---|---|---|---|---|
| FREE RADICAL SUBSTITUTION | x | 80%
| ||
| condition(s) | uv light | 60%
| ||
| halogenoalkane | alcohol | reactant(s) | NaOH/KOH | 44%
|
| ADDITION POLYMERISATION | x | 40%
| ||
| alkane | halogenoalkane | reactant(s) | chlorine/bromine | 32%
|
| halogenoalkane | amine | reactant(s) | ammonia | 24%
|
| halogenoalkane | nitrile | reactant(s) | KCN | 24%
|
| NUCLEOPHILIC SUBSTITUTION | x | 24%
| ||
| ELECTROPHILIC ADDITION | x | 20%
| ||
| ethene | LDPE | temperature (°C) | 200 | 16%
|
| dicarboxylic acid | polyamide | reactant(s) | diamine | 16%
|
| diacyl dichloride | polyamide | reactant(s) | diamine | 16%
|
| additional product(s) | HCl | 16%
| ||
| additional product(s) | HCl | 16%
| ||
| aldehyde | alcohol | reactant(s) | NaBH4 | 16%
|
| ketone | alcohol | reactant(s) | NaBH4 | 16%
|
| additional product(s) | water | 16%
| ||
| additional product(s) | water | 16%
| ||
| CONDENSATION POLYMERISATION | x | 16%
| ||
| ELIMINATION | x | 16%
| ||
| acyl chloride | ester | reactant(s) | alcohol | 12%
|
| dicarboxylic acid | polyester | reactant(s) | diol | 12%
|
| diacyl dichloride | polyester | reactant(s) | diol | 12%
|
| alkene | halogenoalkane | reactant(s) | HBr | 12%
|
| acyl chloride | carboxylic acid | reactant(s) | water | 12%
|
| NUCLEOPHILIC ADDITION | x | 12%
| ||
| ADDITION-ELIMINATION | x | 12%
| ||
| ESTERS | x | 12%
| ||
| reduction of nitrile compounds: | x | 12%
| ||
| ELECTROPHILIC SUBSTITUTION | x | 12%
| ||
| any R group, not just methyl | catalyst(s) | AlCl3 | 8%
| |
| reactant(s) | alcohol | 8%
| ||
| acyl chloride | N-substituted amide | reactant(s) | amine | 8%
|
| acyl chloride | amide | reactant(s) | ammonia | 8%
|
| halogenoalkane | amine | reactant(s) | ammonia | 8%
|
| ester | carboxylic acid, alcohol | reaction name | hydrolysis | 8%
|
| ketone | hydroxynitrile, then carboxylic acid | reactant(s) | KCN | 8%
|
| reactant(s) | NaOH | 8%
| ||
| reactant(s) | water | 8%
| ||
| AMINES | x | 8%
| ||
| friedel-crafts: | x | 8%
| ||
| pressure (atm) | 2000 | 4%
| ||
| any carboxyl group, not just ethanoate | catalyst(s) | AlCl3 | 4%
| |
| additional product(s) | alcohol | 4%
| ||
| alkene | dihalogenoalkane | reactant(s) | bromine | 4%
|
| carboxylic acid | ester | reaction name | esterification | 4%
|
| condition(s) | excess | 4%
| ||
| additional product(s) | HCl | 4%
| ||
| additional product(s) | HCl | 4%
| ||
| 2. nitrile | amine | reactant(s) | hydrogen | 4%
|
| aldehyde | hydroxynitrile, then carboxylic acid | reactant(s) | KCN | 4%
|
| 1. halogenoalkane | nitrile | reactant(s) | KCN | 4%
|
| alkane | alkene | reactant(s) | KOH | 4%
|
| pressure (atm) [not a number] | low | 4%
| ||
| electrophile formed | NO2+ | 4%
| ||
| initiator | oxygen | 4%
| ||
| alcohol | alkene | reactant(s) | phosphoric acid | 4%
|
| ester | salt of a carboxylic acid | reaction name | saponification | 4%
|
| additional product(s) | water | 4%
| ||
| initiator | ziegler-natta catalyst | 4%
| ||
| temperature (°C) | 50 | 0%
| ||
| temperature (°C) | 50 | 0%
| ||
| ethene | HDPE | temperature (°C) | 60 | 0%
|
| condition(s) | acidified with sulfuric acid | 0%
| ||
| condition(s) | acidified with sulfuric acid | 0%
| ||
| [acylation] benzene | phenyl (ethanoate) | reactant(s) | acyl chloride | 0%
|
| additional product(s) | ammonium and chloride ions | 0%
| ||
| additional product(s) | ammonium salt | 0%
| ||
| additional product(s) | ammonium salt and chloride ion | 0%
| ||
| [alkylation] benzene | (methyl)benzene | reactant(s) | chloroalkane | 0%
|
| (hydration) | condition(s) | concentrated | 0%
| |
| condition(s) | concentrated acid | 0%
| ||
| catalyst(s) | concentrated H2SO4 | 0%
| ||
| benzene | nitrobenzene | reactant(s) | concentrated HNO3 | 0%
|
| condition(s) | ethene gas passed through bromine | 0%
| ||
| condition(s) | ethene gas passed through cold concentrated sulfuric acid | 0%
| ||
| condition(s) | ethene gas passed through concentrated HBr | 0%
| ||
| condition(s) | heat under reflux | 0%
| ||
| condition(s) | hot alcoholic solution | 0%
| ||
| (heated under reflux) | condition(s) | hot ethanolic solution | 0%
| |
| (heated under reflux) | condition(s) | hot ethanolic solution | 0%
| |
| condition(s) | in aqueous solution | 0%
| ||
| condition(s) | in aqueous solution | 0%
| ||
| condition(s) | nickel catalyst | 0%
| ||
| why is reduction of nitrile compounds preferred over substitution with halogenoalkanes? | only one desired amine is formed | 0%
| ||
| alkene | alkane | reactant(s) | phosphoric acid | 0%
|
| temperature [not in °C] | room temperature | 0%
| ||
| alkene | alcohol | reactant(s) | sulfuric acid | 0%
|
| condition(s) | warm aqueous solution | 0%
|
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