2) Show an acceptable mechanism for the following transformation using proper curved arrows. HO

Q: Propose a mechanism for the reaction. Fill in the missing curved arrows in each step.

A: The given reaction is of dehydration of alcohol to alkene

Q: Show how to synthesize the molecule on the right, starting from the molecule on the left plus any…

A: A.  first alkyne is reduced partially to alkene by using Lindlar's catalyst. Then it is converted…

Q: HO,

A:

Q: Draw the curved arrow mechanism for the following transformation. Show the mechanism that leads to…

A: NOTE: There is a small error in the reaction. The reactant will be an alkyl halide like bromide and…

Q: ОН

A:

Q: Show the mechanism for this reaction using arrow pushing

A: Friedel craft alkylation  Catalyst AlCl3 Carbocation stability…

Q: Is it possible to synthesize from these two when cutting in this way? Also, please explain the…

A: The provided retrosynthesis will not work for the synthesis of given target molecule. This…

Q: но,

A: Given reaction is amide formation reaction.

Q: Draw the curved mechanism arrows that show the deprotonation of phenol by NaOH and draw the major…

A: This the acid base reaction where NaOH act as  strong base and Phenol acts as a slightly milder…

Q: Please provide a detailed mechanism (with arrows) for this reaction.

A: Here we have to provide the mechanism of synthesis of sulfathiazole-

Q: Show the full mechanism for the following reaction.

A:

Q: Provide a complete mechanism for the following reaction. Pay close attention to details, including…

A:

Q: Show the mechanism in propagation step of monobromination for Compound X below. Compound X

A: Halogenation of alkane: Alkanes can be halogenated in the presence of light or heat. The alkane does…

Q: omplete the following mechanism , show all steps and arrows in full

A: The Fries rearrangement reaction is an organic name reaction which involves the conversion of…

Q: Explain how a student will able to isolate the mono eliminated product in good selectivity used in…

A: products are seperated on the basis of their physical properties.

Q: Synthesis of benzoin

A: Coenzyme synthesis of benzoin

Q: Provide a curved arrow mechanism for the following reaction. NaCl CI

A: Nucleophilic substitution reaction is an organic reaction in which a nucleophile replaces another…

Q: 2. Draw a detailed mechanism for the following reaction.

A:

Q: Write a detailed mechanism f

A: Protonation of alkene  Attack of alkene as nucleophile (intermolecular reaction)   Deprotonation

Q: Br

A:

Q: Using

A: We will give mechanism of the reaction.

Q: H3C-NH2 но. „CH3 H3C-NH2 но. CH3

A: Ans

Q: Provide the appropriate reagent(s) for the following transformation.

A:

Q: Provide the appropriate reagent(s) for the following transformation

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: он CN

A:

Q: Draw the COMPLETE mechanism (including ALL curved arrows and final product) for the reaction below.

A: The given reaction is Diels Alder reaction .This is the type of Cycloaddition reaction .In this…

Q: Which face (axial or equatorial) undergoes reaction with sodium borohydride faster?

A: Sodium borohydride is reducing agent. Sodium brorohydride reacts with ketone to form alcohol.

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: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Which compound below undergoes…

A: Alkenes undergo addition reaction with HBr to form alkyl halide. The H+of HBr acts as an…

Q: arrows

A: Ethylene glycol is a protecting group for carbonyl group and it will give acetal/ketal formation…

Q: Design a reasonable synthesis for the following transformation. + C.

A:

Q: provide CLEAR AND NEAT mechanism with curved arrows for  Part A: Synthesis of benzoin

A: At first HO^- abstract the most active hydrogen from thiamine hydrochloride to get nucleophilic…

Q: Br

A:

Q: Please provide a mechanism with curved arrows for this reaction.

A: Mechanism of Fischer esterification.

Q: This is a retro synthetic analysis problem, shown here is the final product (initial material is…

A:

Q: For each reaction below, show mechanism including curved arrows

A:

Q: PROPOSE AN EFFICIENT SYNTHESIS FOR THE GIVEN TRANSFORMATION

A:

Q: Show all the arrow mechanism including the RIGHT reagents.

A:

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

A:

Q: Show all the arrow-push mechanism including the RIGHT reagents.

A:

Q: Provide a complete curved-arrow mechanism for this transformation

A: The above reaction involves 3 steps. The ester is first alkylated at the alpha position in the…

Q: он CN

A:

Q: Draw a detailed arrow pushing mechanism for the following reaction. In the rate-determining step…

A:

Q: Devise a synthesis of attached compound from the indicated starting material.

A: In this reaction, we have to convert one isomeric form to another isomeric form. For this, we have…

Q: Provide a curved arrow mechanism for the SN1 reaction below: CI CH3 H,C NACN

A: SN1 is a unimolecular nucleophilic substitution reaction. A carbocation is formed after the eviction…

Q: Show all the arrow mechanism including the RIGHT reagents.

A:

Q: Provide an arrow pushing mechanism for the following transformation. Draw out a representation of…

A:

Q: 11. heat -N+-CH3 CH3 12. 1) NaOCH3 H3CO OCH3 2) H*

A:

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.