1. Show the mechanism using curly arrows for the transformation of benzoic acid to benzoyl chloride using SOCI, as a reagent as shown below. CI Benzoic acid Benzoyl chloride

Q: + i) +CH3-MgX H30

A: Grignard reagent :- Alkyl magn esium halide (RMgX)  is called grignard reagent. It is highly polar…

Q: Classify following solvent as protic or aprotic                 CH3NO2

A: Protic solvents are those which contain protons bonded with high electronegative atoms like oxygen…

Q: Which or which of the statements given below is correct. I) Maleic anhydride is a carboxylic acid…

A: (I) Maleic anhydride is a carboxylic acid derivative which on reaction with water gives the…

Q: Write detailed mechanism for pathway from pinacol to pinacolone. You need to use curved arrows to…

A: Pinacol - pinacolone rearrangement is a very important process for the conversion of 1,2-diols into…

Q: Draw a detailed, arrow-pushing mechanism for the conversion of benzoic acid to methyl benzoate under…

A: We have reaction of benzoic acid and methanol to form the methyl benzoate in acidic conditions. We…

Q: 5. Show a correct scheme (show all structures and reagents) that can be used to synthesize…

A: There are many steps involved in synthesising p-chlorophenol from benzene like electrophilic…

Q: HO

A:

Q: Provide the best retrosynthesis nantanol an ner

A:

Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…

A: The Retrosynthesis method is the method that determines the starting material by the fragmentation…

Q: Show two different methods to synthesize alcohol A using a Grignar reaction.

A:

Q: "Using retrosynthetic analysis, provide a synthesis for the fölloWIng reagents next to the arrows…

A: Synthesis: amine fragment can be synthesized from Gabriel synthesis. Acid fragment can be…

Q: Why do we react β-naphthol with ethyl iodide rather than react ethyl alcohol with 2-Iodo…

A: we react β-naphthol with ethyl iodide rather than react ethyl alcohol with 2-Iodo naphthalene

Q: 1. Please draw the retrosynthetic analysis by drawing the immediate precursors to the final product.…

A: find the answer attached

Q: ore Br

A:

Q: + 2 å NaOH

A:

Q: Why do we react β-naphthol with ethyl iodide rather than react ethyl alcohol with 2-Iodo…

A: Perfumes: The Synthesis of Nerolin. Today the pleasant fragrances of perfumes have found their way…

Q: 2. Provide a synthetic approach for the following reactions. Make sure to do the retrosynthetic…

A: the given target molecule is 3° alcohol. This alcohol is prepared from a ketone and grignard…

Q: 1. Draw mechanism (with electron pairs, flow of electrons, charges, and steps, where applicable) of…

A:

Q: Show the arrow pushing mechanism for getting tropylium ion from the benzylic carbocation

A: In the given question we have to rearrange the benzylic carbocation to tropylium ion.

Q: Ph Ph МСРВА Но HO.

A:

Q: When alcohol A is heated with base as shown below, the expected epoxide does not form. Explain why…

A:

Q: Propose a reasonable multi-step synthetic route that would accomplish the following Ph

A:

Q: Show the combination of alcohol and haloalkane that can best be used to prepare   ether by the…

A: Williamson ether synthesis is the method of synthesis of ether by the reaction of alcohol and alkyl…

Q: The saccharide shown here is present in some plant-derived foods.            (a) Indicate the…

A: Given saccharide structure is:

Q: product of Dehydration using sulfiric acid

A: Given compound is a secondary alcohol, which give dehydration Reaction in presence of sulfuric acid.…

Q: 7. Related question a. Draw all theoretically possible aldol condensation products for the following…

A: Please find below all the possible products of the reaction

Q: Please draw the retrosynthetic analysis by drawing the immediate precursors to the final product.…

A: In accordance with the Markovnikov rule, the anionic part of the attacking reagent will go to that…

Q: Draw the major product(s) of nitration of benzoic acid.

A:

Q: Show the process of synthesizing an enolate compound from cyclohexanone using an LDA catalyst.

A:

Q: Draw the synthesis of Ethyl Acetate from ethanol and show its arrow push mechanism.

A:

Q: Provide mechanism with curved arrows for Part B: Synthesis of benzil

A: PhC(=O)-CH(IH)-Ph on oxidation with HNO3 gives Ph-C(=O)-C(=O)-Ph which is called benzil.  At first…

Q: HO3S- -CH3 Br CH3

A: Detail mechanistic pathway is given below to carry out the conversion

Q: 2. Write a synthesis of the Wittig reagent C1

A:

Q: Show the detailed reaction mechanism (symmetrical aldol condensation) of propanal to…

A: Mechanism (symmetrical aldol condensation) of propanal to 2-methyl-2-pentanal for meprobamate.

Q: Provide a curved arrow mechanism for the following reaction. CH;CH>OH + enantiomer

A: This reaction follows SN1 mechanism, In SN1 mechanism firstly leaves group leaves and carbocation…

Q: Devise a stepwise mechanism for the following reaction.

A: Please find below the reaction mechanism

Q: How can I use retrosynthesis to demonstrate how functional groups can be interconverted

A: Retro analysis: Retrosynthesis is the process of “analysing” a target molecule into readily…

Q: Show a mechanism for the conversion of any aldehyde or ketone and any alcohol (as solvent) to the…

A: When an aldehyde or a ketone is treated with an alcohol in present of HCl or any other strong acid…

Q: HO. ОН euryfuran

A: Furan is an organic compound with the oxygen atom present in a five-membered ring. Notably, the…

Q: 4. Provide a retrosynthesis only. Ph Ph Ph Ph

A: Retrosynthesis of the following compounds is given below.

Q: 1) Compare and contrast the similarities and differences between the mechanisms of the carbonyl…

A: According to Q&A guidelines of Bartleby, we are supposed to answer only the first 3 sub-parts of…

Q: Propose a stepwise mechanism for this reaction. The bicarbonate ion will act as a base in the…

A: The given reaction is,

Q: ÇI CI CI, CI CI = ČI OH

A:

Q: B. Give a reasonable synthesis pathway for the transformation below. You may use any organic and…

A:

Q: Provide a retrosynthetic analysis and forward synthesis for the compound shown below. and any other…

A:

Q: Use the malonic ester synthesis to prepare each carboxylic acid.

A: Introduction:Malonic ester synthesis:Malonic ester synthesis: In malonic ester synthesis, diethyl…

Q: 4. Give a short, efficient synthesis of the target compound from the indicated starting material and…

A: The required synthesis is as follows:

Q: What problem(s) might occur if we make the following changes to the work-up procedure of our Ionone…

A: The Ionone synthesis involves the reaction of citral and acetone in the presence of base catalyst to…

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.