Which of the following reagents will react readily with both aldehydes and
ketones?
(a) Grignard reagent
(b) Fehling's reagent
(c) Tollens' reagent
(d) Schiff's reagen

1 Answer

Answer :

Grignard reagent

Related questions

Description : Which of the following statements is NOT correct : (a) Tollens' test is given by both aliphatic and aromatic aldehydes. (b) Fehling's test is given by aliphatic aldehydes. It is not given ... given by methyl ketones and acetaldehydes. (d) Lucas test is given by both aliphatic and aromatic aldehydes

Last Answer : Lucas test is given by both aliphatic and aromatic aldehydes

Description : Ketones react with Grignard reagents to form an addition product which on hydrolysis gives a (a) Primary alcohol (b) Tertiary alcohol (c) Secondary alcohol (d) Ketal

Last Answer : Tertiary alcohol

Description : Benzaldehyde does not react with (a) Tollens' reagent (b) Phenylhydrazine (c) Fehling's solution (d) NaHSO3

Last Answer : Fehling's solution

Description : Benzaldehyde can be distinguished from acetophenone by using : (a) Tollens' reagent (b) Lucas reagent (c) Fehling's reagent (d) All of these

Last Answer : Tollens' reagent

Description : The reagent that can be used to differentiate an aldose and a ketose is : (a) Bromine water (b) Fehling's solution (c) Tollens' reagent (d) None of these

Last Answer : Bromine water

Description : Which of the following statements is false about sucrose? (a) It is also called table sugar. (b) It may be fermented by yeast to produce alcohol. (c) It reduces Fehling's solution. (d) It does not reduce Tollens' reagent.

Last Answer : It reduces Fehling's solution

Description : Which of the following compounds will react with Tollens' reagent to give metallic silver? (a) Formic acid (b) Ethyl alcohol (c) Acetic acid (d) Acetone

Last Answer : Formic acid

Description : Which of the following reagents readily react with ethyl methyl ether? (a) NaOH (b) Conc HI (c) KMnO4 (d) H2O

Last Answer : Conc HI

Description : Indole group of tryptophan responses positively to (A) Glyoxylic acid (B) Schiff’s reagent (C) Biuret test (D) Resorcinol test

Last Answer : Answer : A

Description : Why are aldehydes more reactive than ketones ? 

Last Answer : Ans. It is because of 2 reasons : The carboxyl compounds (both aldehydes & ketones) undergo nucleophilic addition reaction. (i) + I effect : The alkyl group in ketones due to their e- ... its reactivity. (ii) Steric hindrance : Due to steric hindrance in ketones, they are less reactive.

Description : Which of the following characterizes the reactions of aldehydes and ketones? (a) electrophilic addition (b) electrophilic substitution (c) nucleophilic acyl substitution (d) nucleophilic addition; free radical addition

Last Answer : nucleophilic addition; free radical addition

Description : Aldehydes can be distinguished from ketones by using (a) Ammoniacal AgNO3 solution (b) Phenylhydrazine (c) Saturated NaHSO3 solution (d) Thionyl chloride

Last Answer : Ammoniacal AgNO3 solution

Description : Aldehydes undergo oxidation with KMnO4/H+ to give (a) Alcohols (b) Acetals (c) Ketones (d) Acids

Last Answer : Acids

Description : Which statement about the carbonyl group of ketones and aldehydes is true? I. It can attract nucleophiles. II. It can attract electrophiles. III. It tends to undergo addition reactions. IV. It tends to undergo substitution reactions. (a) I and III (b) II and IV (c) I, II, and III (d) I, III, and IV

Last Answer : I, II, and III

Description : Which action best accounts for the solubility of aldehydes and ketones in water? (a) Polar interactions between solute molecules. (b) H-bonding between solute molecules. (c) Van der waals forces (d) H-bonding between solute and solvent molecules

Last Answer : H-bonding between solute and solvent molecules

Description : The melting points of aldehydes and ketones tend to : (a) decrease with increasing molecular weight. (b) increase with increasing molecular weight. (c) remain unchanged with increasing molecular weight. (d) be unpredictable due to resonance

Last Answer : increase with increasing molecular weight.

Description : What property of low-molecular weight aldehydes and ketones accounts for the magnitude of their boiling points? (a) The ability to form strong H-bonds between their molecules. (b) The ability of ... other polar molecules. (d) The ability of the carbonyl group to attract electrophiles and form bonds.

Last Answer : The ability of the polar carbonyl group to attract other polar molecules.

Description : Explain why Grignard reagents do not reacts with alkanes.

Last Answer : Ans. In alkanes , the C – H bond has very little polarity . The hydrogen cannot be abstracted by the Grignard reagent.

Description : Why are Grignard reagents soluble in ether but not in benzene ? 

Last Answer : Ans. Grignard reagents from co-ordination complexes with ether but not benzene since the former has lone pair of electrons but the later does not.

Description : Grignard reagents do not show any reaction with (a) Alkoxyalkanes (b) Alkanones (c) Alkyl alkanoates (d) Acyl halides

Last Answer : Alkoxyalkanes

Description : What is Grignard reagent?

Last Answer : Ans. Alkyl magnesium halides

Description : Which reaction does not yield an ester as one of the products? (a) A carboxylic acid is heated with an alcohol (b) A Grignard reagent is added to a carboxylic acid (c) An acid halide is treated with an alcohol (d) An alkyl halide is heated with the salt of a carboxylic acid

Last Answer : A Grignard reagent is added to a carboxylic acid

Description : Which of the following alcohols can be prepared by the reaction of methyl formate with excess Grignard reagent? (a) 1-pentanol (b) 2-pentanol (c) 3-pentanol (d) 2-methyl-2-pentanol

Last Answer : 3-pentanol

Description : Which of the following is correct? (a) When a Grignard reagent reacts with a ketone, the addition product is a primary alcohol. (b) When a Grignard reagent reacts with a ketone, the addition product ... with a aldehyde, the addition product is a tertiary alcohol. (d) None of the above are correct.

Last Answer : None of the above are correct.

Description : Which of the following reagents can be used to oxidize 1° alcohols to aldehydes? (a) KMnO4 (b) MnO2 (c) K2Cr2O7 (d) PCC

Last Answer : PCC

Description : Which of the following compounds reduces Tollens' reagent? (a) Glucose (b) Sucrose (c) Methanol (d) Acetic acid

Last Answer : Glucose

Description : Acetaldehyde on treatment with Tollens' reagent gives a precipitate of (a) Ag (b) AgNO3 (c) Cu2O (d) None of these

Last Answer : Ag

Description : 1-Butyne can be distinguished from 2-butyne by using (a) potassium permanganate (b) bromine in CCl4 (c) Tollens' reagent (d) chlorine in CCl4

Last Answer : chlorine in CCl4

Description : Ethylene and acetylene can be distinguished by using (a) Bromine in CCl4 (b) Tollens' reagent (b) Baeyer's reagent (d) Phenylhydrazine

Last Answer : Tollens' reagent

Description : A hydrocarbon, C6H12, on ozonolysis gives only one product which does not give silver mirror with Tollens' reagent. The hydrocarbon is (a) 2,3-Dimethyl-2-butene (b) 2-Hexene (c) 2-Methyl-2-pentene (d) 3-Hexene

Last Answer : 2,3-Dimethyl-2-butene

Description : CH3CHO and C6H5CH2CHO can be distinguished chemically by (1) Fehling solution test (2) Benedict test (3) Iodoform test (4) Tollen’s reagent test

Last Answer : Iodoform test

Description : Alcoholic (– OH) group can be identified by : (1) Tollen's Reagent Test (2) Esterification Test (3) FeCl3 Test (4) Ozonolysis Reaction

Last Answer : FeCl3 Test

Description : Grignard reagent is chemically known as (A) Ethyl magnesium chloride (B) Methyl magnesium chloride (C) Dichlorophenol (D) Monochloroacetic acid

Last Answer : (A) Ethyl magnesium chloride

Description : Chemical name of Grignard reagent is (A) Sodium thiosulphate (B) Ethyl magnesium chloride (C) Sodium sulphite (D) Sodium bicarbonate

Last Answer : (B) Ethyl magnesium chloride

Description : The reagent used to test the presence of starch in leaves is – (1) Fehling's solution (2) Iodine solution (3) Million's reagent (4) Benedict's solution

Last Answer : (2) Iodine solution Explanation: The Iodine test is used to test for the presence of starch. Iodine solution — iodine dissolved in an aqueous solution of potassium iodide — reacts with the starch producing a purple black color.

Description : The reagent used to test the presence of starch in leaves is (1) Fehling’s solution (2) Iodine solution (3) Million’s reagent (4) Benedict’s solution

Last Answer : Iodine solution

Description : A reducing sugar will (a) react with Fehling's test (b) not react with Fehling's test (c) have fewer calories (d) always be a ketone

Last Answer : react with Fehling's test

Description : The compound which reacts most readily with Lucas reagent is (a) CH3CH2Cl (b) (CH3)2CHOH (c) CH3CH2OH (d) (CH3)3COH

Last Answer : (CH3)3COH

Description : Which of the following reagents will react with furan to form 2-furansulfonic acid? (a) SO3 in pyridine at 100°C (b) Dilute H2SO4 at 200°C (c) SO2 at 100°C (d) Dilute H2SO4 at 100°C

Last Answer : SO3 in pyridine at 100°C

Description : Which of the following reagents will react with pyrrole to form 2- formylpyrrole? (a) HCOOH (b) CHCl3/KOH (c) H2O2 (d) (CH3CO)2O/SnCl4

Last Answer : CHCl3/KOH

Description : Which of the following reagents does not react with aniline? (a) Acetyl chloride (b) Acetic anhydride (c) Ammonia (d) Nitrous acid

Last Answer : Ammonia

Description : Which of the following reagents will react with methyl group rather than the benzene ring in methylbenzene? (a) Chlorine in the presence of uv light (b) CH3Cl in the presence of AlCl3 (c) CH3COCl in the presence of AlCl3 (d) Hydrogen in the presence of nickel

Last Answer : Chlorine in the presence of uv light

Description : Which of the following reagents will react with acetamide to form methylamine? (a) LiAlH4 (b) Br2/NaOH (c) PCl5 (d) H2/Ni

Last Answer : Br2/NaOH

Description : Which of the following reagents will react with propene? (a) Hot alkaline KMnO4 (b) Sodium metal (c) Cold dilute HNO3 (d) LiAlH4

Last Answer : Hot alkaline KMnO4

Description : Alldehydes and Ketones react with `NH_(2)OH` to form aldoximes and Ketoximes respectively. Configuration of these can be determined by Beckmann rearra

Last Answer : Alldehydes and Ketones react with `NH_(2)OH` to form aldoximes and Ketoximes respectively. Configuration of these can be ... A. I B. II C. III D. IV

Description : Alldehydes and Ketones react with `NH_(2)OH` to form aldoximes and Ketoximes respectively. Configuration of these can be determined by Beckmann rearra

Last Answer : Alldehydes and Ketones react with `NH_(2)OH` to form aldoximes and Ketoximes respectively. Configuration of these can be ... A. I B. II C. III D. IV

Description : Aniline undergoes oxidation with Na2Cr2O7/H2SO4 to give (a) Schiff's base (b) p-Benzoquinone (c) Phenol (d) Benzoic acid

Last Answer : p-Benzoquinone

Description : Two aliphatic aldehydes P and Q react in th presence of aqueous `k_(2)CO_(3)` to give compound R, which upon treatment with HCN provides compound S. O

Last Answer : Two aliphatic aldehydes P and Q react in th presence of aqueous `k_(2)CO_(3)` to give compound R, which ... shown below: The compound S is B. C. D.

Description : Two aliphatic aldehydes (P) and (Q) react in the presence of aqueous `K_(2)CO_(3)` to give compound (R ) which upon treatment with HCN gives compound(

Last Answer : Two aliphatic aldehydes (P) and (Q) react in the presence of aqueous `K_(2)CO_(3)` to give compound (R ) ... (P) and (Q), respectively, are: B. C. D.