| Hint | Answer | % Correct |
|---|---|---|
| Alcohols can react with carboxylic acids to form _ using eg. concentrated sulfuric acid or concentrated phosphoric acid. (1) | Esters (1) | 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 _ (2) | Alcoholic alkoxides (2) | 0%
|
| _ can react with acid chlorides to form esters using no catalyst | Alcohols | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with aqueous alkalis to form _ (1) | Alcohols (1) | 0%
|
| Alkenes can undergo acid catalysed hydration (electrophilic addition) to form _ (2) | Alcohols (2) | 0%
|
| Aldehydes and ketones can undergo reduction by eg. lithium aluminium hydride to form _ (3) | Alcohols (3) | 0%
|
| _ can undergo dehydration to form alkenes, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or concentrated phosphoric acid (4) | Alcohols (4) | 0%
|
| _ can react with metals such as sodium or potassium to form alcoholic alkoxides (5) | Alcohols (5) | 0%
|
| _ can be oxidised using eg. acidified permanganate, acidified dichromate, or hot copper (II) oxide (6) | Alcohols (6) | 0%
|
| _ can react with carboxylic acids to form esters using eg. concentrated sulfuric acid or concentrated phosphoric acid. (7) | Alcohols (7) | 0%
|
| _ can undergo reduction by eg. lithium aluminium hydride to form alcohols | Aldehydes and ketones | 0%
|
| Alkenes can take part in electrophilic addition reactions with hydrogen to form _ in the presence of a catalyst | Alkanes | 0%
|
| _ can undergo acid catalysed hydration (electrophilic addition) to form alcohols | Alkenes | 0%
|
| Alcohols can undergo dehydration to form _, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or concentrated phosphoric acid (1) | Alkenes (1) | 0%
|
| Monohaloalkanes can undergo base-induced elimination of hydrogen halides to form _ (2 | Alkenes (2) | 0%
|
| _ can take part in electrophilic addition reactions with hydrogen to form alkanes in the presence of a catalyst (3) | Alkenes (3) | 0%
|
| _ can take part in electrophilic addition reactions with halogens to form dihaloalkanes (4) | Alkenes (4) | 0%
|
| _ can take part in electrophilic addition reactions with hydrogen halides to form monohaloalkanes (5) | Alkenes (5) | 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%
|
| Monohaloalkanes can undergo _-induced elimination of hydrogen halides to form alkenes | Base | 0%
|
| Nitriles can be hydrolysed to form _ (1) | Carboxylic acids (1) | 0%
|
| Alcohols can react with _ to form esters using eg. concentrated sulfuric acid or concentrated phosphoric acid. (2) | Carboxylic acids (2) | 0%
|
| Alcohols can undergo dehydration to form alkenes, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or _ (1) | Concentrated phosphoric acid (1) | 0%
|
| Alcohols can undergo dehydration to form alkenes, using a catalyst such as aluminium oxide, _ , or concentrated phosphoric acid (1) | Concentrated sulfuric acid (1) | 0%
|
| Alcohols can react with carboxylic acids to form esters using eg. concentrated sulfuric acid or _ (2) | Conc. phosphoric acid | 0%
|
| Alcohols can react with carboxylic acids to form esters using eg. _ or concentrated phosphoric acid. (2) | Conc. Sulphuric acid (2) | 0%
|
| Alcohols can undergo _ to form alkenes, using a catalyst such as aluminium oxide, concentrated sulfuric acid, or concentrated phosphoric acid | Dehydration | 0%
|
| Alkenes can take part in electrophilic addition reactions with halogens to form _ | Dihaloalkanes | 0%
|
| Alkenes can take part in _ reactions with hydrogen to form alkanes in the presence of a catalyst | Electrophilic addition | 0%
|
| Alkenes can take part in _ reactions with halogens to form dihaloalkanes (2) | Electrophilic addition (2) | 0%
|
| Alkenes can take part in_ reactions with hydrogen halides to form monohaloalkanes (3) | Electrophilic addition (3) | 0%
|
| Alkenes can undergo acid catalysed hydration (_) to form alcohols (7) | Electrophilic addition (7) | 0%
|
| Monohaloalkanes can undergo base-induced _ of hydrogen halides to form alkenes | Elimination | 0%
|
| Alcohols can react with acid chlorides to form _ using no catalyst (2) | Esters (2) | 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%
|
| Monohaloalkanes can undergo base-induced elimination of _ to form alkenes (1) | Hydrogen halides (1) | 0%
|
| Alkenes can take part in electrophilic addition reactions with _ to form monohaloalkanes (2) | Hydrogen halides (2) | 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 aqueous alkalis to form alcohols (1) | Monohaloalkanes (1) | 0%
|
| _ can take part in nucleophilic substitution reactions with alcoholic alkoxides to form ethers (2) | Monohaloalkanes (2) | 0%
|
| _ can take part in nucleophilic substitution reactions with ethanolic cyanide to form nitriles (3) | Monohaloalkanes (3) | 0%
|
| Alkenes can take part in electrophilic addition reactions with hydrogen halides to form_ (4) | Monohaloalkanes (4) | 0%
|
| Monohaloalkanes can take part in nucleophilic substitution reactions with ethanolic cyanide to form _ (1) | Nitriles (1) | 0%
|
| _ can be hydrolysed to form carboxylic acids (2) | Nitriles (2) | 0%
|
| Alcohols can react with acid chlorides to form esters using _ | No catalyst | 0%
|
| Monohaloalkanes can take part in _ reactions with aqueous alkalis to form alcohols (1) | Nucleophilic Substitution (1) | 0%
|
| Monohaloalkanes can take part in _ reactions with alcoholic alkoxides to form ethers (2) | Nucleophilic substitution (2) | 0%
|
| Monohaloalkanes can take part in _ reactions with ethanolic cyanide to form nitriles (3) | Nucleophilic substitution (3) | 0%
|
| Alcohols can be _ using eg. acidified permanganate, acidified dichromate, or hot copper (II) oxide | Oxidised | 0%
|
| Alcohols can react with metals such as sodium or _ to form alcoholic alkoxides | Potassium | 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%
|