4) Devise a synthesis of the molecule below from the given sources. You may use any reag need along with the starting material. Me. .N. „Me Me HO H. MeO OMe N. Me O

Q: Question ? Provide a synthesis of the given target compound from the given starting material. OH L…

A:

Q: What is a multi-step synthesis with intermediate steps to produce the following molecule?

A: Multi-step synthesis of this molecule:The IUPAC name is 4, 5 dichloro 6, 6 dimethyl octane. The…

Q: ОН

A:

Q: What is the needed reagent to perform the following reaction? OH ???

A: Alkenes are the organic compounds which contain atleast one double bond present in it. It can be…

Q: 3.1 Propose a detailed mechanism for the reaction below: CI AICI 3

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Q: 4. Devise a multi-step synthesis using Chem 241 reactions only a) CH b) c)

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Q: O CH3CCH₂CH₂CH3 NaBH4/CH3OH

A: NaBH4 acts as a reducing agent by providing H- ion . It reduces Aldehyde into a primary alcohol and…

Q: 5.3 Propose a mechanism for the reaction below: H

A: The reaction between Ketone with the amine in the presence of Acid , we get the addition product of…

Q: Make a SynthesiS Starting S HCECH + materials w l'Carbon and any necessary reagents

A: The synthesis route for preparation of 2,6-octadiene is given by

Q: OH

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Q: ropose a mechanism for the following reaction: s H3C CH3 H3C- CH3 + (CH3)2NH H3C H3C `N CH3 CH3 H3C…

A: Given compound is organic compound as it contain carbon and hydrogen atoms.

Q: Identify a more stable tautomer from the following enol and keto tautomers. Explainyour answer…

A: Phenol is an aromatic Organic compound, with Molecular formula of C6H5OH. It exist as first aromatic…

Q: O Br Br O OMe NH₂

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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 for below product from the given starting material. More than one step is…

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Q: OH ONLY CI

A: See synthesis below.

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: . Show how the enamine below can be synthesized. Then draw the resonance structure(s) for the…

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Q: 2. propose a Synthotic soute Cinclude rectancts/cegeants/solvents etc.) to Your molecule from…

A: Given compound is propanoyl chloride.  Let's see synthesis of this molecule from ethylene.

Q: Br

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. Pl +O°H Select to Draw

A: This is a hydrolysis reaction being carried out in presence of acid to form alcohol. The formation…

Q: Devise a synthesis of the given trans vinylborane, which can be used for bombykol synthesis. All of…

A: Catecholborane is used to synthesize the starting material of Suzuki reaction. The reaction of…

Q: CO, Me

A: This compound:                                                                     can be…

Q: Propose a mechanism for the reaction shown below

A: Please find below the reaction mechanism.

Q: Proposed a mechanism to determine the final product NEN CIO

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Q: LOCH3

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

Q: OH 7.

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Q: What is the major product of the following reaction? (Note that the triangle under the reaction…

A: In the given question we have to do the elimination reaction in presence of base NaOMe to form more…

Q: A. Propose a short synthesis for the following molecule. You can start with acetylene, and alkyl…

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Q: HN CH3B H,0 H* (cat)

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Q: Provide a synthesis of the following target from the given starting material. from OH

A: The carboxylic acid can be first converted to the shown compound as follows:

Q: b) Provide a working synthesis for the transformation. 1. CH3LI 2, H20 OH OEt H' CH3

A: Methyl lithium is higher reactive than the Grignard reagent. Methyl lithium reacts with the given…

Q: For C, D and E, determine which step undergo the elimination, substitution or additor State the…

A: Given : We have to choose reagents for each step.

Q: Propose a mechanism for the reaction shown below:

A: Firstly, the proton abstraction by the oxygen atom of the -OH group will occur. This will lead to…

Q: Me carbons units of 3 or fewer Me Me Me

A: synthesis of the given product

Q: edict the major product for the following reaction, by proposing a plausible stepwise mechanism.…

A: In this question we want to draw major product with mechanism.  You can see the major product in…

Q: ОН Br ОН

A: For synthesis, first we have to block acid and alcohol group as ester and ether respectively .…

Q: ggest an efficient synthesis for the following product starting from the correspondi rting material…

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Q: What is the needed reagent to perform the following reaction? ??? Select one: O a. CI Ob CH;CH,CH,…

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Q: How would I use Gabriel synthesis here?

A: Gabriel synthesis:

Q: Choose the best reagents to complete the reaction shown below. P Tyne here to search

A:

Q: A)

A: Here we have to prepare the following given compounds from alkyl halide containing four carbon atom…

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: a syntho tic soute Cinclude rectancts/cegeants/solvents etc.) propose to Your molecule from paroblem…

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: Instructions: a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B…

A: Given information,

Q: OH ??? Meo OMe

A: Phenol  oxidation  is done by a specific oxidizing  reagent  with help of conc acid as explained  in…

Q: H₂O /H₂SO4 HgSO4 NaBH4/CH3OH

A: Given reaction is :  Predict the products of the reaction ?  According to Markovnikov's rule,…

Q: но, b) 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.