Chemistry
Chemical Reactions and Equations
674 Questions
Chemical reactions and equations form a foundational chemistry topic where students identify reaction products, balance chemical formulas, and classify reaction types. It covers critical mechanisms like Markovnikov's rule, precipitation, and endothermic or exothermic processes. These questions are highly common in general science sections of state and central government competitive exams.
Endothermic reactionsPrecipitation reactionsDehydrohalogenation of alkyl halidesChemical equation balancingReaction product identification
Chemical Reactions and Equations Questions
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n-Bromosuccinimide
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tert-Butanesulphinamide
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tert-Butyl hydroperoxide
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fluorenylmethyloxycarbonyl chloride
A
Correct answer
Explanation
N-Bromosuccinimide or NBS is a chemical reagent which is used in radical substitution and electrophilic addition reactions in organic chemistry. NBS can be considered a convenient source of cationic bromine.
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n-Butyllithium
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tert-Butyllithium
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Caesium acetate
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Carbon tetraiodide
C
Correct answer
Explanation
Caesium acetate is an ionic caesium compound often used in organic synthesis especially in Perkin synthesis; formation of unsaturated cinnamic-type acids by the condensation of aromatic aldehydes with fatty acids.
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1,8-Diazabicyclo[5.4.0]undec-7-ene
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Dibutylboron trifluoromethanesulphonate
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Dichloromethyl methyl ether
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Diethyl azodicarboxylate
A
Correct answer
Explanation
1,8-Diazabicyclo[5.4.0]undec-7-ene or more commonly DBU, is a chemical compound and belongs to the class of amidine compounds. It is used in organic synthesis as a catalyst and complexing ligand and a strong (pKa = 24.34 in acetonitrile) non-nucleophilic base.
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Dimethyl malonate
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Diethyl malonate
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4-Dimethylaminopyridine
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Dimethyldioxirane
C
Correct answer
Explanation
4-Dimethylaminopyridine is a derivative of pyridine. This colourless solid is a useful nucleophilic catalyst for a variety of reactions such as esterifications with anhydrides, the Baylis-Hillman reaction, hydrosilylations, tritylation, the Steglich rearrangement, Staudinger synthesis of β-lactams and many more. vv
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Ethyl 2-bromoacetate
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Ethyl chloroformate
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Ethyl diazoacetate
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Benzyl chloroformate
A
Correct answer
Explanation
Ethyl 2-bromoacetate is the ethyl ester of bromoacetic acid. It is used as a lachrymatory agent and tear gas agent for chemical warfare.
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Dansyl chloride
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Di-tert-butyl dicarbonate
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2,6-Di-tert-butylpyridine
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1,5-Diazabicyclo[4.3.0]non-5-ene
C
Correct answer
Explanation
2,6-Di-tert-butylpyridine is a pyridine derivative. In organic chemistry, it is used as a hindered base.
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Bis(chloromethyl) ether
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(Bis(trifluoroacetoxy)iodo)benzene
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Bis(trimethylsilyl)acetamide
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Bis(trimethylsilyl)amine
B
Correct answer
Explanation
(Bis(trifluoroacetoxy)iodo)benzene is a hypervalent iodine compound used as a reagent in organic chemistry. The reagent is used in an acidic modification of the Hofmann rearrangement. One example is the conversion of cyclobutanecarboxamine to cyclobutylamine hydrochloride.
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Transmetalation
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Carbometalation
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Hydrometalation
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Alkyne trimerisation
D
Correct answer
Explanation
An alkyne trimerisation reaction is a 2+2+2 cyclisation reaction in which three alkyne molecules react to form an aromatic compound. The reaction is 'pseudo' pericyclic since it has not been observed to occur without the assistance of metal catalysis; and the metal catalyst assembles the ring stepwise via intermediates which are not directly in between (in a geometric sense) the starting material and products.
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Both A and R are true and R is the correct explanation of A.
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Both A and R are true but R is NOT the correct explanation of A.
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A is true but R is false.
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A is false but R is true.
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Both A and R are false.
B
Correct answer
Explanation
This option is correct, because in styrene, carbon atom attached to phenyl group is designated as α-carbon while that carrying Cl-atom is designated as β-carbon.
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Both A and R are true and R is the correct explanation of A.
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Both A and R are true but R is NOT the correct explanation of A.
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A is true but R is false.
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A is false but R is true.
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Both A and R are false.
A
Correct answer
Explanation
Benzaldehyde forms two oximes on reacting with NH2OH because the two oximes arise due to geometrical isomerism around C=N bond. Thus, this option is correct.
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Oxidative addition
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Beta-hydride elimination
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Transmetalation
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Carbometalation
C
Correct answer
Explanation
Transmetalation is a general chemical reaction type in organometallic chemistry describing the exchange of ligands between two metal centers. The metal centers need not be the same. The ligands R and R' can be organic or inorganic. The double displacement reaction is conceptually related. Transmetalation is important in the synthesis of various organometallic compounds.
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Both A and R are true and R is the correct explanation of A.
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Both A and R are true but R is NOT the correct explanation of A.
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A is true but R is false.
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A is false but R is true.
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Both A and R are false.
C
Correct answer
Explanation
This option is correct because CH3CO group in acetophenone being electron withdrawing reduces the electron density in the benzene ring-thereby preventing further electrophilic substitution.
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Only A
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Only B
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Only C
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A and C
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A, B and C
A
Correct answer
Explanation
This option is correct, because Corey-House reaction can be used to prepare both alkenes with odd and even number of carbon atoms.
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Only A
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Only B
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Only C
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A, B and C
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None of these
A
Correct answer
Explanation
This option is correct, because in two step reaction, the rate determining step has the highest energy of activation.
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hydroquinone
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Quinol and catechol
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Ortho-hydroxyacetophenone and para-hydroxyacetophenone
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Anisole
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Ethyl chloride and ethyl acetate
B
Correct answer
Explanation
This option is correct. Phenol when oxidised in presence of potassium persulphate, it gives quinol and catechol.