Interpretation:
To accomplish the target products transformation should be draw and identified, using particular reagents.
Concept introduction:
Nucleophilic reaction: electron rich nucleophiles attacks the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.
Acid Catalyzed Hydration Reaction: The reaction involves breaking of π-bonds between carbon-carbon multiple bonds and addition of alcohol to more substituted position of carbon in the molecule.
Grignard Reaction: This is a organometallic reaction in different alkyl, aryl-magnesium halides add to a carbonyl group in an
Wittig reaction: This process allows the preparation of an alkene by the reaction of an aldehyde (
Oxidation Reaction: The oxidation-reduction reaction is a type of
Ozonolysis Reaction: It is an oxidative reaction which is used to oxidize the carbon-carbon double and triple bond. Several type organic of reactions where the unsaturated bonds of
Anti-Markovnikov addition: These rules describe the regioselectivity (particular place in functional group) where the substituent is bonded to a less substituted carbon, rather than the more substituted carbon. This placed is quite unusual as carbon cations which are commonly formed during alkene or alkyne reactions tend to favor the more substituted carbon.
Markovnikov addition: The addition reaction of parotic acids to a different alkene or alkyne, the hydrogen atom of
To identify: The synthetic route to accomplish the given transformation.
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