1) Nucleophilic substitution reaction of alkyl halide is a process when nucleophile replace the leaving group of alkyl halide. Propose the mechanism and product(s) for the following substitution reaction.

Q: Reduction reaction of 1-phenylethanone with lithium aluminium hydride yields a racemic mixture of…

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Q: Suppose you are told that each reaction is a substitution reaction but are not told the mechanism.…

A: The chemical reaction in which one functional group is substituted by another functional group is…

Q: What are the Possible Mechanisms for Nucleophilic Substitution ?

A: The replacement of any atom or group of atoms by a nucleophile is known as nucleophilic substitution…

Q: Assume that attached starting materials can be converted to an epoxide by this reaction. Draw the…

A: The general mechanism for Ether formation is as follows:

Q: مع مسن NO₂ NaCN CN NO₂ Although aromatic substitution reactions usually occur by an electrophilic…

A: The rule for electron flow is that electron flows from electron rich center or bond to electron…

Q: Alkyl halides undergo nucleophilic substitution and elimination reactions. When the kinetics of the…

A: The given reaction gives the nucleophilic substituted product as well as elimination product.

Q: Based on the characteristics of the carbonyl group (C = O), what reactions or transformations take…

A: Carbonyl group consist of electropositive and electronegative atom bonded with double bond. Because…

Q: Write a mechanism that accounts for the formation of ethyl isopropyl ether as one of the products in…

A: Addition reactions are basically the reaction in which addition of any nucleophile or electrophile…

Q: Write the mechanism of the reaction of 3-Methyl-1-pentene with HBr

A: The products that are formed in the reaction between 3-Methyl-1-pentene with HBr are shown below.

Q: Arrange the following compounds in increasing order of their property as indicated :(i) CH3COCH3,…

A: Most important reactions of carbonyl compound are Nucleophilic addition reaction, where an electron…

Q: What reaction converts nitrobenzene to 1-bromo-3-nitrobenzene Alkylation Acylation Halogenation…

A: Br is halogen , in the reaction halogenation occur

Q: This is a transesterification reaction. It mechanistically is the same as a Fischer Esterification.…

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Q: Write the mechanism of the aliphatic nucleophilic substitution reaction between n-butanol and Br- in…

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Q: Give the mechanism of friedel craft alkylation of benzene

A: Friedel-Crafts Alkylation refers to the replacement of an aromatic proton with an alkyl group. This…

Q: Specify the reaction conditions to favour the indicated elimination mechanism. a. Strong base, such…

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Q: Predict the product that forms upon reaction of 1-methylcyclohexene with iodine monochloride, I-Cl,…

A: When alkene or alkyne react with hydrogen halide it gives alkylhalide (haloalkane) as a product.…

Q: The reaction between ethanoyl chloride and the hydroxide ion to give an acid is classified as:…

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Q: Provide the major organic product of the following reaction. but-1-ene H₂O, H+ What type of…

A: Here we have to predict the type of regiochemistry observed in hydration of but-1-ene in presence of…

Q: On a piece of paper, provide a two-step reaction pathway for the synthesis of the product X using a…

A: The alkene is known as a molecule with a double bond. When the double bond resides in a cyclic ring,…

Q: What reaction converts 1-bromo-3-nitrobenzene to 3-bromoaniline Alkylation Acylation Halogenation…

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Q: Which alkynyl halide will most rapidly give a substitution product at C1 upon reaction with a…

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Q: O The Wolf-Kishner reduction is a reaction used in Organic Chemistry to convert carbonyl…

A: The overall chemical reaction of Wolf-Kishner reduction is:

Q: Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the…

A: The reaction of cyclohexanol with Lewis acid BF3 would be given as, The above step is the first…

Q: Give two sets of reactants (each set including an alkyl halide and a nucleophile) that could be used…

A: Please find below the first set of reactants

Q: what will be the type of interaction of ethane with bromine: a) radicals b) ionic c) nucleophilic d)…

A: Halogenation of Alkanes occurs when any alkane (ethane) reacts with bromine.

Q: How you can synthesize methylacetylene (at least two methods). Write reactions of methylacetylene…

A: Methyl acetylene is C3H4, three Carbon in a chain containing one single C-C bond and a triple C-C…

Q: In the addition reactions of alkynes, the reagents undergo transformation to form first. a. a…

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Q: Give two sets of reactants (each set including an alkyl halide and a nucleophile) that could be used…

A: Please find below the first set of reactants

Q: Provide the reagents necessary to complete the following reactions. More than one step may be…

A: In this question, we have to synthesized the product from given reactant by using necessary…

Q: Alkylation of benzene with 1-chlorobutane in the presence of AlCl3 gave not only the expected…

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Q: For the base-catalysed hydrolysis of 3-bromo-3-methylhexane (i.e. reaction with the nucleophile…

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Q: Suppose you are told that each reaction is a substitution reaction but are not told the mechanism.…

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Q: Alkene + Reagent

A: Given is reaction of alkene.

Q: When 2-methylpent-2-eno reacts with HCl two alkyl halides are formed. Present the structures of the…

A: When alkene is treated with HCl them π bond breaks and carbocation formed then  Cl- attacks on that…

Q: Identify the correct structure of the alkene which gives the two electophilic addition products with…

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Q: Provide the curved-arrow mechanism to account for the following nucleophilic addition reaction. H20…

A: Hydrolysis of amine to nitrile is nucleophilic addition reaction. And mechanism for this reaction…

Q: The following are intermediate products in the stepwise synthesis of compound 1 from benzene. Give…

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Q: Write the mechanisms for the following reactions bellow, justifying each substitution position.

A: The first part is electrophilic chlorination. The chlorination occurs ortho and para to the acetyl…

Q: Nucleophilic aromatic substitution provides one of the common methods for making phenols. Show how…

A: Conversion of benzene  to p-nitro phenol -  In this reaction along with the para product ortho…

Q: Provide the name of the product after cyclopropanone reacts with methylmagnesium bromide and…

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Q: Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the…

A: Naphthalene undergoes electrophilic aromatic substitution in the first position. The structure of…

Q: HNO3, H₂SO4 Electrophile Intermediate -H* N

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Q: Acid-catalysed dehydration of 2,2-dimethyleyclohexanol yields, in part, isopropylidenecyclopentane.…

A: To find two carbonation generated during reaction

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.