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