Please provide a synthetic route for this molecule CH3 Ome

Q: what is the product and mechanism used in this reaction? MsO DBU CH₂Cl2

A: -> DBU acts as a base to abstract a proton from a beta carbon adjacent to a leaving group in a…

Q: 5) Use a curved arrow notation mechanism to show how each product is formed in the following…

A: Given reaction is : Use the curved arrow notation to show how each product is formed in the…

Q: 2. Draw a reaction mechanism to explain the following reaction. OH (aq) LOH i. OH

A: We have to show the mechanism for the above given reaction in which a compound having epoxide ring…

Q: Draw a stepwise, detailed mechanism for the following reaction. CH3NH2 N-CH3 CH,NH, Cr (excess)

A: When nitrogen atom is bonded with three carbon atom is known as tertiary amine.

Q: Give detailed Solution..show work..don't give Handwritten answer..don't use Ai for answering this

A: Therefore this given number is 7 figures.Explanation:

Q: in nucleophilic acyl substitution,

A: In this question we have to choose correct option of the under basic conditions, in nucleophilic…

Q: Draw a step-wise mechanism for the following substitution reaction. Be sure to add lone pairs and…

A:

Q: Draw a veasonable mechanism for this reaction that involves free radicals. CoH hv DH cat. OH Ph H,C

A:

Q: Q10. Propose a plausible mechanism for the given transformation. Ignore stereochemistry. H NaOMe I…

A:

Q: b. HO,

A: Solution: a) the given compound is tertiary alcohol. So can be prepared from either Alkene or…

Q: 20) Draw a stepwise, detailed mechanism for the following reaction. Use curved arrows to show the…

A:

Q: MeH, Ме ОН N. Fill in the necessary reagents to complete the given reaction. ZI

A: Here we have to synthesize the following given compounds by using suitable reagents through…

Q: 22. OH HO Br

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: What is the product of the following sequence of reactions? NaOH NaNH2 H3O+ NH2 IV ||

A: An E2 elimination takes place where a chloroalkane is transformed into alkene. At first the Acidic…

Q: Show arrow pushing mechanism for the following reaction. OH OH Br2 Br. Br H2O Br

A: The given reaction scheme is shown below.We have to provide the arrow pushing mechanism of the above…

Q: Which of the following reagents can do conjugate addition?

A: A conjugate addition with a nucleophile as carbanion (C-) is known as the Michael addition or…

Q: Circle the correct reactant to make the following epoxide. LIG OH X OH Ph 4 Br OH OH Ph Ph "OH H LA

A:

Q: HO Д HC но 0 0 одн

A:

Q: Draw the product when attached compound is treated with either (CH3)2CuLi, followed by H2O, or…

A: The reagent, (CH3)2CuLi, is an organocuprate reagent, also called Gilman Reagent. Its general form…

Q: 3D0

A:

Q: Draw the product when attached compound is treated with either (CH3)2CuLi, followed by H2O, or…

A: The organocuprate reagents undergo 1,4-addition where a CH3 group is added at the β-carbon.

Q: Propose an efficient synthesis CI MeO O OMe OEt COOH Br NO₂ O EtO

A: We have to propose an efficient synthesis.

Q: Show a possible mechanism for the following reaction CN CO,Me CN.

A:

Q: Draw the mechanism using the appropriate arrows for the following reaction. OH H₂SO4 H₂O +

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw a step-wise mechanism for the following substitution reaction. Be sure to add lone pairs and…

A: The reactions in which  an atom or a group of atoms are replaced  by another atom or group of atoms…

Q: c) Propose a mechanism for this reaction. BF3 Но HO.

A: BF3 , boron triflouride is lewis acid. So lone pair of oxygen of -OH group attack on it and…

Q: Select the correct reagent for the following transformation

A:

Q: Draw the product when attached compound is treated with either (CH3)2CuLi, followed by H2O, or…

A: The product when attached compound is treated with either (CH3)2CuLi, followed by H2O, or HC≡CLi,…

Q: Provide the product for SN1 mechanism. Br CH3 CH₂CH3 NOH

A: The reaction proceeds by the SN1 reaction mechanism. The first step of the SN1 reaction is the…

Q: ) Starting from benzent synthesig the fo lloning compounds. çootH NO2 NO2 NO2 Br

A: the synthetic route of the given product fro benzene are provided in attach image.

Q: Can you explain the mechanism for this question HO OH H2SO4 cat. H₂O

A:

Q: 2 3 OH Provide missing reagents Provide missing reagents OH Br

A: Given are organic synthesis reactions.Let's find out missing reagents for each,

Q: Synthesize from Br но Br OH

A: The reaction of a bromo compound with sodium hydroxide (NaOH) to form an alkene is known as the…

Q: 2. Fill in the missing reagent and/or product for each of the following reactions. 2 요 H OEt H. CHO…

A: Question involves name reactions that is condensation reaction to form carbon-carbon bond .

Q: mechanism pattern involved in this reaction is loss of a leaving group rearrangement nucleophilic…

A:

Q: Draw the major product(s) when the following molecule is reacted with excess NaOEt in EtOH, followed…

A: The reaction is one the best example to illustrate the combination reaction in the presence of a…

Q: Draw a reasonable mechanism for this reaction: -он E. H* H H -ӧн но: но H -ÖH :0: HO- HÖ- O :ÖH 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.