(a)
Interpretation: The reagents used to convert the methylcyclohexane into given molecules should be identified.
Concept Introduction:
Addition Reaction: It is defined as
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.
Anti-Markovnikov’s Addition Rule: The unsymmetrical
Acid Catalyzed Hydration Reaction: The reaction involves breaking of phi bonds between carbon-carbon multiple bonds and addition of alcohol to more substituted position of carbon in the molecule.
Radical Bromination: It is a type of bromination which proceeds via radical chain mechanism.
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical
Hydroboration reaction: The reaction involves addition of
To identify: The reagents used to convert the given molecule.
(b)
Interpretation: The reagents used to convert the methylcyclohexane into given molecules should be identified.
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.
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.
Anti-Markovnikov’s Addition Rule: The unsymmetrical alkene in a chemical compound reacts with hydrogen halide in a way, where halide ions attacks and bond to the less substitution position of carbon-carbon double bond.
Acid Catalyzed Hydration Reaction: The reaction involves breaking of phi bonds between carbon-carbon multiple bonds and addition of alcohol to more substituted position of carbon in the molecule.
Radical Bromination: It is a type of bromination which proceeds via radical chain mechanism.
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical
Hydroboration reaction: The reaction involves addition of
To Find: To identify the reagents used in the given conversion.
(c)
Interpretation: The reagents used to convert the methylcyclohexane into given molecules should be identified.
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.
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.
Anti-Markovnikov’s Addition Rule: The unsymmetrical alkene in a chemical compound reacts with hydrogen halide in a way, where halide ions attacks and bond to the less substitution position of carbon-carbon double bond.
Acid Catalyzed Hydration Reaction: The reaction involves breaking of phi bonds between carbon-carbon multiple bonds and addition of alcohol to more substituted position of carbon in the molecule.
Radical Bromination: It is a type of bromination which proceeds via radical chain mechanism.
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical
Hydroboration reaction: The reaction involves addition of
To Find: To identify the reagents used in the given conversion.
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