devise synthesis for the following reaction. Br HO CN

Q: ОН

A:

Q: Select the major product in the following reaction.

A: Solution: We know tertiary butoxide is a strong hindered base. Given substrate is tertiary alkyl…

Q: Br

A: Organic Transformation  First  Hydro Halo Elimination followed by Cis Hydroxylation to give cis…

Q: OH .CI

A: Answer: This conversion can be performed in two step where dehydrohalogenation of Alkyl halide is…

Q: Provide the structure of the major product which results from the following reaction. CN

A:

Q: Plan a synthesis of congored?

A: Congo red is an organic compound and is a type of an azo dye, it is a water soluble compound and…

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

A: The synthesis of given compound from the indicated starting material can be shown as follows,

Q: Devise a synthesis of attached alkyne. You may use acetylene, benzene,organic halides, ethylene…

A: The given compound can be synthesized from the specified reagents following a series of reaction:…

Q: Devise a synthesis of each compound from benzene.

A: Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: + en

A:

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

A: The starting material of the synthesis of compound is phenol. The structure of the final product…

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: A stepwise and detained mechanism for the given reaction can be shown below,

Q: DHG (OACameay

A: The above-given reaction is an example of Oxymercuration demarcation reaction:

Q: OH

A:

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: The given reaction is,

Q: A) Propose an efficient synthesis for the following transformation: + en B) Propose an efficient…

A: To propose an efficient synthesis for the following transformation:

Q: Br "cEN,

A: Cyanide ion is a weak base and a strong nucleophile. So, It will react with 2-bromocyclohexanone via…

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

A: Given: To prepare: cis-1,2- dimethoxycyclohexane  from cyclohexene

Q: The following hemiacetal is synthesized from wh

A: Carbonyl compounds undergo " nucelophilic addition reactions "  Carbonyl compounds are two types…

Q: Provide a method to synthesize from the shown compounds. Br НО.

A: Solution-   Step 1st and step 2nd Grignard reagent synthesis and Grignard reaction. step-3; acid to…

Q: Draw the major organic product of the reaction conditions shown

A:

Q: Show how the anisole can be synthesized from benzene:

A: Anisole is a methoxy group attached to the benzene ring.

Q: Starting with benzene and using any other necessary reagents of your choice,design a synthesis…

A: The given product is formed from benzene by using the following three steps.

Q: LOCH3

A: Synthesize the given synthesis starting from the starting compounds using the necessary organic and…

Q: Draw the major organic product for the reaction shown.

A: The given reactant molecule is 3,3-dimethyl butanal. The reduction of an aldehyde with sodium…

Q: Select the major product of the following reaction.

A: Electrophilic addition reactions (EAR):  In general alkenes undergo electrophilic addition…

Q: Draw the major organic product of the reaction shown.

A: The reaction proceeds in two steps.  In the first step, a proton is added to the hydroxyl group to…

Q: Но from

A: 1. Diethyl malonoate has active methylene H's these are acidic in nature , which is abstracted by…

Q: Synthesize attacged compound from the given starting materials?

A: For the attached compound the product obtained is aryl-halide from the biphenyl is actually a…

Q: НО. HI

A:

Q: See attached file

A: An efficient synthesis for the following transformation, therefore the reaction of cyclic…

Q: HO

A:

Q: CI .CI Br

A: The given reaction is represented as follows:

Q: оссH2CH3

A:

Q: Propose a synthesis for   compound from benzene

A:

Q: Draw a stepwise, detailed mechanism for the following reaction.

A:

Q: ОН

A: Alcohols can be converted to corresponding alkanes. This can be achieved either by  (i) converting…

Q: Provide a synthesis for the following reaction. If more than one step is required be sure to number…

A: The reaction taking place is given as,

Q: a) ホ→ OMe b)

A: Number of functional group is associated with organic compounds which impart specific chemical and…

Q: Draw the major product of the following reaction. CI OMe

A:

Q: How do I do this?

A:

Q: Propose a mechanism for the following reaction:

A: In organic chemistry, there is a class of reactions that belongs to rearrangement reactions. This…

Q: How would I use Gabriel synthesis here?

A: Gabriel synthesis:

Q: ropose an efficient synthesis for the following transformation: Br

A: In given reaction bromobenzene is converted into styrene.

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

A: Benzene is an aromatic compound which contain electron density and is attacked by the electrophiles.…

Q: S O NaBH4 OLIAIH4 OBH3, THF OLIAIH(O'Bu) 3 OH

A: Organic reactions are those in which organic reactant react to form organic products.

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: Propose an efficient synthesis for the given transformation. +En

A:

Q: Draw a stepwise, detailed mechanism for the following intramolecular reaction that forms a cyclic…

A: The given reaction is  To find: The stepwise mechanism for the given intramolecular 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.