The target molecules should be drawn and identified for the given statements by using its starting molecule. Concept introduction: Addition Reaction: It is defined as chemical reaction in which two given molecules combines and forms product. The types of addition reactions are electrophilic addition, nucleophilic addition, free radical additions and cycloadditions. Generally, compounds with carbon-hetero atom bonds favors addition reaction. Nucleophilic reaction : electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction. Elimination Reaction: It is just reverse reaction of addition where substituent from the given molecule is removed via E1 (the reaction depends only on the substrate involved in the reaction) or E2 (the reaction depends on both of the substituents in the reaction) mechanism. Meta-chloroperoxybenzoic acid (m-CPBA): This reagent is extremely useful reagent most frequently encountered in the synthesis of epoxides when added to alkenes or alkynes . 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 alkenes, alkynes or azo compounds are cleaved with ozone. Hydrolysis Reaction: This type of reaction involving the braking of a carbon-carbon triple, double bonds in a molecules using water. LAH Reduction: The saturated/unsaturated aldehyde and ketones in the presence of sodium metal in LAH and carbonyl compound produced saturated alcohols. The keto group involves in the reduction process of LAH, this end up reducing to give the alcohols. Oxidation Reaction : The oxidation-reduction reaction is a type of chemical reaction it is involves a transfer of electrons between two species. In other words oxidation reaction number of a molecule atom or ion changes by gaining or losing electrons. To identify: The given synthetic route to accomplish the target molecule transformation.

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Chapter 19, Problem 53PP

Interpretation Introduction

Interpretation:

The target molecules should be drawn and identified for the given statements by using its starting molecule.

Concept introduction:

Addition Reaction: It is defined as chemical reaction in which two given molecules combines and forms product. The types of addition reactions are electrophilic addition, nucleophilic addition, free radical additions and cycloadditions. Generally, compounds with carbon-hetero atom bonds favors addition reaction.

Nucleophilic reaction: electron rich nucleophiles attack the positive or partially positive charge of an atom and replace a leaving group is called Nucleophilic Substitution reaction.

Elimination Reaction: It is just reverse reaction of addition where substituent from the given molecule is removed via E1 (the reaction depends only on the substrate involved in the reaction) or E2 (the reaction depends on both of the substituents in the reaction) mechanism.

Meta-chloroperoxybenzoic acid (m-CPBA): This reagent is extremely useful reagent most frequently encountered in the synthesis of epoxides when added to alkenes or alkynes.

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 alkenes, alkynes or azo compounds are cleaved with ozone.

Hydrolysis Reaction: This type of reaction involving the braking of a carbon-carbon triple, double bonds in a molecules using water.

LAH Reduction: The saturated/unsaturated aldehyde and ketones in the presence of sodium metal in LAH and carbonyl compound produced saturated alcohols. The keto group involves in the reduction process of LAH, this end up reducing to give the alcohols.

Oxidation Reaction: The oxidation-reduction reaction is a type of chemical reaction it is involves a transfer of electrons between two species. In other words oxidation reaction number of a molecule atom or ion changes by gaining or losing electrons.

To identify: The given synthetic route to accomplish the target molecule transformation.

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