Interpretation: The product M of the given two-step reaction sequence is to be identified.
Concept Introduction: The addition of a halogen to an
The replacement or substitution of one
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- Show how to bring about each step in this synthesis of the herbicide propranil.arrow_forwardThe formation of Br2 from NBS first involves the reaction of NBS with HBr to form an iminol intermediate and molecular bromine. The intermediate then undergoes acid-catalyzed tautomerism to form succinimide, the byproduct of the reaction. Propose a curved-arrow mechanism for the conversion of NBS into succinimide that also accounts for the formation of Br2.arrow_forwardTollen’s reagent reacts with acetic acid which leads to the formation of silver precipitate. Explain the molecular basis.arrow_forward
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- For the following monosubstituted benzenes, (a) determine whether the group is strongly, moderately, or weakly activating or deactivating, (b) write the three possible products for the reaction, and (c) predict which of these three products you would expect to predominatearrow_forwardWhen CO2 is bubbled through a solution of benzyl magnesium bromide, and the mixture is then acidified, the product is phenylacetic acid. Any unreacted benzyl magnesium bromide is converted to toluene in the acidification step. 1. Write the complete reaction sequence for the process, showing product and byproduct. 2. How could you separate phenylacetic acid from toluene?arrow_forwardIn a mixture of the two reactants, HNO3 and methyl benzoate, the nitration of methyl benzoate O Would form primarily methyl para-nitrobenzoate. O Would form primarily methyl meta-nitrobenzoate. O Would not take place. O Would form primarily methyl ortho-nitrobenzoate.arrow_forward
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