Sr. # | Questions | Answers Choice |
---|---|---|
1 | Which acid is used in the manufacture of synthetic fibre | Formic acid Phthalic acid Carbonic acid Acetic acid |
2 | Carboxylic acids generally exists in cyclic | Monomers Dimers Trimers Tetrameter |
3 | When a carboxylic acid reacts with a metal ______ gas is evolved | H<sub>2</sub> CO<sub>2</sub> CI<sub>2</sub> None of these |
4 | Acidic amino acid Basic amino acid Neutral amino acid None of these | |
5 | Essential amino acids are those amino acids which | Body can not synthesize Body can synthesize <span style="color: rgb(34, 34, 34); font-family: "Times New Roman"; font-size: 24px; text-align: center; background-color: rgb(255, 255, 248);">α</span>-amino acids <span style="color: rgb(34, 34, 34); font-family: "Times New Roman"; font-size: 24px; text-align: center; background-color: rgb(255, 255, 224);">β</span>-amino acids |
6 | Proton donar Dehydrating agent Catalyst Electrophile | |
7 | Easter are pleasant smelling compounds. Which ester posseses odour like pineapple | Amylacetate Amylbutyrate Ethylbutyrate Benzylacetate |
8 | Alkyl Alkyl nitrile Cyanogens Amine | |
9 | The acids obtained by the hydrolysis of fats and oils are called | Active compound Fatty acids Functional group None |
10 | Monocarboxylic acids exist as dimer because of | Dipole-dipole attraction Hydrogen bonding Van der Waals forces Conhesive forces |
11 | With the increase in carbon no. the solubility of carboxylic acids | Increases Decreases Remains same None of these |
12 | Carboxylic acid can generally be prepared by various methods. Which of the following methods is not suitable for making carboxylic acids | By the oxidation of primary alcohols By the hydrolysis of nitriles By the carbonation of Grignard, reagent By the hydrolysis of p-amines |
13 | The common name of propanoic acid is | Acetic acid Formic acid Propionic acid Butyric acid |
14 | A common industrial solvent is a mixture of propanone; CH3COCH3, and pentyl ethanoate CH3CO2(CH2)4CH3. Which reagent would have no effect on this solvent | Na<sub>(s)</sub> NaBH<sub>4</sub> NaOH<sub>(aq)</sub> 2,4-dinitrophenylhydrazine reagent |
15 | Which of these reactions is shown by buranone, CH3COCH2CH3 | On warming with acidified potassium dichromative (IV) the solution turns green On heating with Fehling's reagent a red precipitate is formed With 2,4-dinitrophenlhydrazine reagent an orange precipitate is formed With hydrogen cyanide an aldehyde is formed |
16 | With H<sub>2</sub>/Ni CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CH<sub>2</sub>OH With H<sub>2</sub>/Ni CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CH<sub>3</sub> With NaBH<sub>4</sub> CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CH<sub>2</sub>OH With NaBH<sub>4</sub> CH<sub>3</sub>(CH<sub>2</sub>)<sub>5</sub>CHO | |
17 | Q and R Q and R R only Q and R Q and R R only Q only R only | |
18 | Which compound would undergo nucleophilic addition | Ethene, C<sub>2</sub>H<sub>4</sub> Bromoethane, C<sub>2</sub>H<sub>5</sub>Br Ethanal, CH<sub>3</sub>CHO Ethane, C<sub>2</sub>H<sub>6</sub> |
19 | Ethanal may be converted into a three-carbon acid in a two-step process. Which compound is the intermediate |
CH<sub>3</sub>CO<sub>2</sub>H CH<sub>3</sub>CN CH<sub>3</sub>CH<sub>2</sub>CN CH<sub>3</sub>CH(OH)CN |
20 | A compound R has all of the following properties. It is neutral; It gives an orange precipitate with 2,4-dinitrophenythydrazine; it evolves hydrogen chloride when treated with PCI5in the cold What could R be | |
21 | Which compound on reaction with hydrogen cyanide produces a compound with a chiral centre | Ch<sub>3</sub>CHO CH<sub>3</sub>CH<sub>2</sub>COCH<sub>2</sub>CH<sub>3</sub> CH<sub>3</sub>CO<sub>2</sub>CH<sub>3</sub> HCHO |
22 | Aldehydes and ketones are carbonyl compounds. Which of them react both with NaBH4and with Tollen's reagent | Both aldehydes and ketones Aldehydes only Ketones only Neither aldehydes nor ketones |
23 | ||
24 | Which alcohol may be oxidised to a product which react with 2,4-dinitorphenylhydrazine reagent but not with Fehling's reagent | Butan-1-ol Butan-2-ol 2-methylpropan-1-ol 2-methylpropan-2-ol |
25 | What is formed when propanone is refluxed with an anhydrous solution of NaBH4 | Propanal Propan-1-ol Propan-2-ol Propane |
26 | In 1903 Arthur Lapeworth became the first chemist to investigate a reaction mechanism. The reaction he investigated was that of hydrogen cyanide with propanone. What do we now call the mechanism of this reaction | Electrophilic addition Electrophilic substitution Nucleophilic addition Nucleophilic substitution |
27 | Compounds X, Y and Z, all react with PCI5to release hydrogen chloride, but only one of them reacts eith 2,4-dinitrophenylhydrazine reagent. Which one of the following combinations could be X, Y and Z | |
28 | Which reagent could be used to distinguish between CH3CH(OH)CH2CHO and CH3COCH2CH2OH | Acidified potassium dichromate Dilute sulphuric acid 2,4-dinitrophenylydrazine Fehling's reagent |
29 | Br<sub>2(aq)</sub> 2, 4-dinitrophenylhydrazine NaBH Tollen's reagent | |
30 | Which isomer of C5H11OH gives, one dehydration, the greastest number of different alkenes |