4 Questions
Match the following with their corresponding definition:
SN1 reaction = Substitution nucleophilic unimolecular SN2 reaction = Substitution nucleophilic bimolecular SNi reaction = Substitution nucleophilic intramolecular Stereochemistry = The nucleophile can attack from either face of the planar carbocation intermediate
Match the following with the correct representation:
2-bromo-2-methylpropane with water = 2-methylpropan-2-ol & hydrogen bromide tert-butyl bromide solvolysis = Tertiary butyl alcohol Carbocation intermediate = Trigonal planar Oxonium ion formation = Reaction of the carbocation with water
Match each reaction with its primary characteristic:
First order kinetics = Kinetic order of SN1 reaction Rate-determining step = Formation of carbocation in SN1 reaction Concentration dependency = Rate of SN1 reaction Leaving group dissociation = Step 1 in solvolysis of tert-butyl bromide
Match the following mechanisms with the corresponding reactions:
Attack of nucleophile from either face = Stereochemistry explanation Dissociation of leaving group to form a carbocation = Step 1 in solvolysis of tert-butyl bromide Proton transfer to complete the reaction = Step 3 in solvolysis of tert-butyl bromide Reaction of carbocation with water to form oxonium ion = Step 2 in solvolysis of tert-butyl bromide
Test your knowledge on electrophilic aromatic substitution reactions involving benzene, as well as addition reactions where two reactants combine to form a single product. Explore examples like the nitration of benzene and regeneration of catalysts in chemical reactions.
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