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