Chapter 21, Problem 54PP

Interpretation Introduction

Interpretation:

The given reagents used to accomplish the target products (major product) transformation should be draw and 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.

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.

$S_{N}1$Reaction: The $S_{N}1$ reaction is twostep process, leaving group leaves the molecule is first step and forms the more stable carbocation. Further, nucleophile attacks the carbocation and forms the final product in the second step. The rate of the reaction depends on the stability of the carbocation.

$S_{N}2$Reaction: The $S_{N}2$ reaction is single step process, leaving group leaves the molecule and nucleophiles attack the molecule is single step process which is simultaneous process.

Grignard Reaction: This is a organometallic reaction in different alkyl, aryl-magnesium halides add to a carbonyl group in an aldehyde and ketone. This reaction is an important for the conversion of carbon-carbon single $\left(-C-C-\right)$ bond. Moreover the addition of a reagent to an aster, lactone gives a tertiary alcohol in which will alkyl groups are the same and the addition of a Grignard reagent to a nitrile produces an unsymmetrical ketone.

Halogenation: The addition of halogen atoms to a $\text{π-}$ conjunction system. The several unsaturated organic compounds like, alkenes, alkynes and cyclohexenes that has one double bond is halogenated, the resulting molecules is completely saturated or halogenated.

Friedel-Crafts alkylation:  This reaction electrophilic aromatic substitution allows the synthesis of monoacylated $\left(R-CO-C{H}_3\right)$ products from the reaction between arenes and acyl chlorides (or) anhydrides. The obtained products are deactivated and go not undergo a second substitution place.   (or) This type of reaction involves of an aromatic ring with an alkyl halide using strong Lewis acid catalyst $\left(AlC{l}_3\right)$ or anhydrous $FeC{l}_3$ as a catalyst, the alkyl group attaches at the former site of the chlorine atoms.

Sodium amide ( ${\text{NaNH}}_{\text{2}}$): The strong base of ${\text{NaNH}}_{\text{2}}$ will deprotonate alkynes, alcohols and other organic functional groups with acidic protons such as esters and ketones. It is also a very strong nucleophile. It is a strong base and excellent nucleophile. It’s used deprotonated of weak acids and also for elimination reaction.