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Edexcel A level Organic Chemistry Reactions - Statistics
General Stats
-
This quiz has been taken 5 times
4 since last reset
- The average score is 1 of 47
Answer Stats
| Hint | Answer | % Correct |
|---|---|---|
| alkane to halogenoalkane | halogen, UV light | 100%
|
| primary amine to salt | acid | 33%
|
| ester to alcohol and carboxylic acid | acid hydrolysis, dilute sulfuric acid, reflux | 0%
|
| carboxylic acid to primary alcohol | acidified lithium aluminium hydride in dry ether | 0%
|
| nitrile to primary amine | acidified lithium aluminium hydride in dry ether | 0%
|
| alkene to diol | acidified potassium manganate | 0%
|
| friedel-craft acylation | acyl chloride, aluminium chloride catalyst, reflux | 0%
|
| primary amine to n-substituted amide | acyl chloride, hydrogen chloride byproduct, may form an ammonium salt | 0%
|
| acyl chloride to ester | alcohol, hydrogen chloride byproduct | 0%
|
| carboxylic acid to ester | alcohol, sulfuric acid catalyst, reflux | 0%
|
| Grignard reagent to secondary alcohol | aldehydes, dry ether, dilute hydrochloric acid | 0%
|
| acyl chloride to amide | ammonia, hydrogen chloride byproduct | 0%
|
| halogenoalkane to alcohol | aqueous potassium hydroxide, reflux | 0%
|
| ester to alcohol and carboxylate salt | base hydrolysis, dilute sodium hydroxide, reflux | 0%
|
| bromination of benzene | bromine, iron (iii) bromide catalyst, reflux | 0%
|
| bromination of phenol | bromine water, RTP | 0%
|
| Grignard reagent to carboxylic acid | carbon dioxide, dry ether, dilute hydrochloric acid | 0%
|
| alcohol to ester | carboxylic acid, sulfuric acid catalyst, reflux | 0%
|
| chlorination of benzene | chlorine, aluminium chloride catalyst, reflux | 0%
|
| alcohol to alkene | concentrated phosphoric acid catalyst, 170C | 0%
|
| alcohol to chloroalkane | concentrated phosphorus pentachloride | 0%
|
| nitration of benzene | concentrated sulfuric acid catalyst, concentrated nitric acid, below 55C | 0%
|
| primary amine to complex ion with copper ions | copper (ii) sulfate | 0%
|
| nitrile to carboxylic acid | dilute hydrochloric acid, reflux | 0%
|
| primary alcohol to aldehyde/carboxylic acid | dilute sulfuric acid, potassium dichromate, reflux | 0%
|
| secondary alcohol to ketone | dilute sulfuric acid, potassium dichromate, reflux | 0%
|
| primary amine to basic solution | dissolve in water | 0%
|
| aldehyde to hydroxynitrile | ethanolic hydrogen cyanide, reflux | 0%
|
| halogenoalkane to nitrile | ethanolic potassium cyanide,reflux | 0%
|
| halogenoalkane to alkene | ethanolic potassium hydroxide, reflux | 0%
|
| halogenoalkane to primary amine | excess, ethanolic ammonia, reflux, sealed flask | 0%
|
| friedel-craft alkylation | halogenoalkane, aluminium chloride catalyst, reflux | 0%
|
| alkene to dihalogenoalkane | halogen, RTP | 0%
|
| alkene to halogenoalkane | hydrogen halide, RTP | 0%
|
| alkene to alkane | hydrogen, nickel catalyst, 150C | 0%
|
| Grignard reagent to tertiary alcohol | ketones, dry ether, dilute hydrochloric acid | 0%
|
| halogenoalkane to Grignard reagent | magnesium, dry ether, reflux | 0%
|
| Grignard reagent to primary alcohol | methanal, dry ether, dilute hydrochloric acid | 0%
|
| nitration of phenol | nitric acid, RTP | 0%
|
| carboxylic acid to acyl chloride | phosphorus pentachloride | 0%
|
| alcohol to bromoalkane | potassium bromide in 50% concentrated sulfuric acid catalyst | 0%
|
| alcohol to iodolkane | potassium triiodide made in-situ using red phosphorus and iodine | 0%
|
| acyl chloride to n-substituted amide | primary amine, hydrogen chloride byproduct, may form an ammonium salt | 0%
|
| alkene to alcohol | steam, phosphoric acid catalyst, 300C, 70atm | 0%
|
| nitrobenzene to phenylamine | tin and concentrated hydrochloric acid, reflux, add sodium hydroxide | 0%
|
| primary amine to higher order amine | warmed, excess, ethanolic halogenoalkane | 0%
|
| acyl chloride to carboxylic acid | water, hydrogen chloride byproduct | 0%
|
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