Carboxylic acid - Quiz
A) Citrate synthase B) Fatty acid synthase C) Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCo) D) Acetyl-CoA carboxylase
A) Propionic acid B) Terephthalic acid C) Citric acid D) Acetic acid
A) Carboxylate salts B) Polyamides of aminocarboxylic acids C) Polymers D) Esters of fatty acids
A) Hydroformylation of alkenes B) Oxidation of aldehydes with air C) Cativa process (carbonylation of alcohols) D) Hydrocarboxylation of alkenes
A) Acrylic acid B) Phthalic acid C) Benzoic acid D) Terephthalic acid
A) Adipic acid B) Propionic acid C) Acetic acid D) Citric acid
A) Citric acid B) Propionic acid C) Acrylic and methacrylic acids D) Adipic acid
A) Fermentation of ethanol B) Oxidation of primary alcohols C) Soap making D) Carbonation of Grignard reagents
A) Ethylenediaminetetraacetic acid B) Maleic acid C) Acetic acid D) Citric acid
A) Benzoic acid B) Terephthalic acid C) Phthalic acid D) Acrylic acid
A) Hydrocarboxylation of alkenes B) Fermentation of ethanol C) Carbonylation of alcohols D) Oxidation of aldehydes with air
A) Acetic acid B) Propionic acid C) Adipic acid D) Citric acid
A) Terephthalic acid B) Phthalic acid C) Salicylic acid D) Benzoic acid
A) Benzoic acid B) Acrylic acid C) Phthalic acid D) Terephthalic acid
A) Citric acid B) Propionic acid C) Adipic acid D) Ethylenediaminetetraacetic acid
A) Acrylic acid B) Terephthalic acid C) Benzoic acid D) Maleic acid
A) Carboxylate salts B) Polyamides of aminocarboxylic acids C) Esters of fatty acids D) Polymers
A) Propionic acid B) Citric acid C) Fatty acids D) Adipic acid
A) Ketones B) Amides C) Esters D) Carboxylic acids
A) R−COOH or R−CO2H B) R−OH C) R−CHO D) R−NH2
A) Amino group (−NH2) B) Hydroxyl group (−OH) C) Aldehyde group (−CHO) D) Carboxyl group (−C(=O)−OH)
A) Position one B) Position three C) Position two D) Position four
A) Acetone B) Acetic C) Acetate D) Acetyl
A) Due to their high molecular weight B) Due to their nonpolar nature C) Due to their large molecular size D) Due to their ability to hydrogen bond with water
A) They yield water-soluble sodium salts B) They form esters C) They form insoluble sodium salts D) They decompose into alcohols and ketones
A) Due to their nonpolar nature B) Due to their ionic nature C) Due to their high solubility in nonpolar media D) Due to their tendency to self-associate through hydrogen bonding
A) Low solubility (0.2 g/L) B) High solubility C) Moderate solubility D) Complete insolubility
A) A carboxylic ketone B) A carboxylic alcohol C) A carboxylic ester D) A carboxylate anion
A) -ous B) -ic C) -ide D) -ate
A) Acts as a hydrogen-bond acceptor B) Acts as a hydrogen-bond donor C) Acts as an electron donor D) Acts as an electron acceptor
A) Acts as a hydrogen-bond acceptor B) Acts as an electron acceptor C) Acts as a hydrogen-bond donor D) Acts as an electron donor
A) They decompose B) They do not ionise C) They completely ionise D) They partially ionise (dissociate)
A) They ionise B) They dissolve completely C) They exist as dimers D) They decompose
A) It is the functional group B) It is a substituent C) It is a side chain D) It is a solvent
A) Partially soluble B) Insoluble C) Soluble D) Completely insoluble
A) R−COO− or R−CO−2 B) R−CHO C) R−OH D) R−COOH
A) Proton (H+) donors. B) Proton (H+) acceptors. C) Electron donors. D) Electron acceptors.
A) Fischer esterification reaction B) Von Richter reaction C) Kolbe–Schmitt reaction D) Cannizzaro reaction
A) Von Richter reaction B) Kolbe–Schmitt reaction C) Cannizzaro reaction D) Benzilic acid rearrangement
A) Cannizzaro reaction B) Kolbe–Schmitt reaction C) Fischer esterification reaction D) Von Richter reaction
A) ATP B) Diazomethane C) Sodium bicarbonate D) Phenols
A) Sodium bicarbonate B) Nitrobenzenes C) Diazomethane D) Phenols
A) Cannizzaro reaction B) Benzilic acid rearrangement C) Von Richter reaction D) Kolbe–Schmitt reaction
A) Phosphorus(III) chloride B) Thionyl chloride C) Lithium aluminium hydride D) Grignard reagents
A) Lithium aluminium hydride B) Grignard reagents C) Thionyl chloride D) Organolithium compounds
A) Alcohol B) Aldehyde C) Ketone D) Acid chloride
A) Organolithium compounds B) Vilsmaier reagent C) Thionyl chloride D) Lithium aluminium hydride
A) Phosphorus acid B) Phosphorus(V) oxychloride C) Sulfur dioxide D) Hydrogen chloride
A) Thionyl chloride B) Phosphorus(V) chloride (PCl5) C) Lithium aluminium hydride D) Phosphorus(III) chloride (PCl3)
A) Grignard reagents B) Organolithium compounds C) Vilsmaier reagent D) Lithium aluminium hydride
A) Vilsmaier reagent B) Thionyl chloride C) Lithium aluminium hydride D) Phosphorus(III) chloride
A) Alcohols B) Aldehydes C) Ketones D) Esters
A) Hell–Volhard–Zelinsky halogenation B) Schmidt reaction C) Kolbe electrolysis D) Arndt–Eistert synthesis
A) Fukuyama reduction B) Kolbe electrolysis C) Rosenmund reduction D) DIBAL reduction
A) Oxidative decarboxylation B) Conversion to amines C) Reduction to alcohols D) Decarboxylative dimerization |
Created with That Quiz —
the math test generation site with resources for other subject areas.