| Hint | Answer | % Correct |
|---|---|---|
| _ can react with carboxylic acids to form esters using eg. concentrated sulfuric acid or concentrated phosphoric acid. | Alcohols | 100%
|
| Aldehydes and ketones can undergo reduction by eg. lithium aluminium hydride to form _ | Alcohols | 100%
|
| _ can undergo reduction by eg. lithium aluminium hydride to form alcohols | Aldehydes and ketones | 100%
|
| Alkenes can take part in electrophilic addition reactions with hydrogen to form _ in the presence of a catalyst | Alkanes | 100%
|
| Monohaloalkanes can undergo _-induced elimination of hydrogen halides to form alkenes | Base | 100%
|
| Alcohols can undergo _ to form alkenes, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or concentrated phosphoric acid | Dehydration | 100%
|
| Monohaloalkanes can undergo base-induced _ of hydrogen halides to form alkenes | Elimination | 100%
|
| Alkenes can take part in electrophilic addition reactions with hydrogen halides to form_ | Monohaloalkanes | 100%
|
| _ can take part in nucleophilic substitution reactions with ethanolic cyanide to form nitriles | Monohaloalkanes | 100%
|
| Alcohols can react with metals such as sodium or _ to form alcoholic alkoxides | Potassium | 100%
|
| Alkenes can undergo _ catalysed hydration (electrophilic addition) to form alcohols | Acid | 0%
|
| Alcohols can react with _ to form esters using no catalyst | Acid chloride | 0%
|
| Alcohols can be oxidised using eg. acidified permanganate, _ , or hot copper (II) oxide | Acidified dichromate | 0%
|
| Alcohols can be oxidised using eg. _, acidified dichromate, or hot copper (II) oxide | Acidified permanganate | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with _ to form ethers | Alcoholic alkoxides | 0%
|
| Alcohols can react with metals such as sodium or potassium to form _ | Alcoholic alkoxides | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with aqueous alkalis to form _ | Alcohols | 0%
|
| _ can react with acid chlorides to form esters using no catalyst | Alcohols | 0%
|
| _ can react with metals such as sodium or potassium to form alcoholic alkoxides | Alcohols | 0%
|
| _ can undergo dehydration to form alkenes, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or concentrated phosphoric acid | Alcohols | 0%
|
| _ can be oxidised using eg. acidified permanganate, acidified dichromate, or hot copper (II) oxide | Alcohols | 0%
|
| Alkenes can undergo acid catalysed hydration (electrophilic addition) to form _ | Alcohols | 0%
|
| Alcohols can undergo dehydration to form _, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or concentrated phosphoric acid | Alkenes | 0%
|
| _ can undergo acid catalysed hydration (electrophilic addition) to form alcohols | Alkenes | 0%
|
| _ can take part in electrophilic addition reactions with halogens to form dihaloalkanes | Alkenes | 0%
|
| _ can take part in electrophilic addition reactions with hydrogen halides to form monohaloalkanes | Alkenes | 0%
|
| _ can take part in electrophilic addition reactions with hydrogen to form alkanes in the presence of a catalyst | Alkenes | 0%
|
| Monohaloalkanes can undergo base-induced elimination of hydrogen halides to form _ (2 | Alkenes | 0%
|
| Alcohols can undergo dehydration to form alkenes, using a catalyst such as _, concentrated sulfuric acid, or concentrated phosphoric acid | Aluminium oxide | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with _ to form alcohols | Aqueous alkalis | 0%
|
| Alcohols can react with _ to form esters using eg. concentrated sulfuric acid or concentrated phosphoric acid. | Carboxylic acids | 0%
|
| Nitriles can be hydrolysed to form _ | Carboxylic acids | 0%
|
| Alcohols can undergo dehydration to form alkenes, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or _ | Concentrated phosphoric acid | 0%
|
| Alcohols can undergo dehydration to form alkenes, using a catalyst such as aluminium oxide, _ , or concentrated phosphoric acid | Concentrated sulfuric acid | 0%
|
| Alcohols can react with carboxylic acids to form esters using eg. concentrated sulfuric acid or _ | Conc. phosphoric acid | 0%
|
| Alcohols can react with carboxylic acids to form esters using eg. _ or concentrated phosphoric acid. | Conc. Sulphuric acid | 0%
|
| Alkenes can take part in electrophilic addition reactions with halogens to form _ | Dihaloalkanes | 0%
|
| Alkenes can take part in _ reactions with halogens to form dihaloalkanes | Electrophilic addition | 0%
|
| Alkenes can take part in_ reactions with hydrogen halides to form monohaloalkanes | Electrophilic addition | 0%
|
| Alkenes can take part in _ reactions with hydrogen to form alkanes in the presence of a catalyst | Electrophilic addition | 0%
|
| Alkenes can undergo acid catalysed hydration (_) to form alcohols | Electrophilic addition | 0%
|
| Alcohols can react with acid chlorides to form _ using no catalyst | Esters | 0%
|
| Alcohols can react with carboxylic acids to form _ using eg. concentrated sulfuric acid or concentrated phosphoric acid. | Esters | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with _ to form nitriles | Ethanolic cyanide | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with alcoholic alkoxides to form _ | Ethers | 0%
|
| Alkenes can take part in electrophilic addition reactions with _ to form dihaloalkanes | Halogens | 0%
|
| Alcohols can be oxidised using eg. acidified permanganate, acidified dichromate, or _ | Hot copper (II) oxide | 0%
|
| Alkenes can undergo acid catalysed _ (electrophilic addition) to form alcohols | Hydration | 0%
|
| Alkenes can take part in electrophilic addition reactions with _ to form alkanes in the presence of a catalyst | Hydrogen | 0%
|
| Alkenes can take part in electrophilic addition reactions with _ to form monohaloalkanes | Hydrogen halides | 0%
|
| Monohaloalkanes can undergo base-induced elimination of _ to form alkenes | Hydrogen halides | 0%
|
| Nitriles can be _ to form carboxylic acids | Hydrolysed | 0%
|
| Aldehydes and ketones can undergo reduction by eg. _ to form alcohols | Lithium aluminium hydride | 0%
|
| _ can undergo base-induced elimination of hydrogen halides to form alkenes | Monohaloalkanes | 0%
|
| _ can take part in nucleophilic substitution reactions with alcoholic alkoxides to form ethers | Monohaloalkanes | 0%
|
| _ can be hydrolysed to form carboxylic acids | Nitriles | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with ethanolic cyanide to form _ | Nitriles | 0%
|
| Alcohols can react with acid chlorides to form esters using _ | No catalyst | 0%
|
| Monohaloalkanes can take part in _ reactions with ethanolic cyanide to form nitriles | Nucleophilic substitution | 0%
|
| Monohaloalkanes can take part in _ reactions with alcoholic alkoxides to form ethers | Nucleophilic substitution | 0%
|
| Monohaloalkanes can take part in _ reactions with aqueous alkalis to form alcohols | Nucleophilic Substitution | 0%
|
| Alcohols can be _ using eg. acidified permanganate, acidified dichromate, or hot copper (II) oxide | Oxidised | 0%
|
| Aldehydes and ketones can undergo _ by eg. lithium aluminium hydride to form alcohols | Reduction | 0%
|
| Alcohols can react with metals such as _ or potassium to form alcoholic alkoxides | Sodium | 0%
|