Propose a multi step synthesis to the product shown using the starting material given and any other reactions!reagent needed

Q: . onow how to carry out each of the following conversio reagents you want. Draw the product after…

A: We can use m-CPBA for epoxidation of alkene.

Q: 1-Draw the mechanism of 1-methylcyclohexene with hydrogen bromide please.     2-Draw the reaction…

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: Synthesis – any reagents needed H

A: This synthesis can be done by multiple addition elimination followed by oxidation.

Q: Draw the major organic product(s) of the following reactions

A: (g) With alpha hydrogen containing carbonyl compounds inpresence of dil.base give beta-hydroxy…

Q: Devise a synthesis of each compound from the indicated starting material. You may also use any…

A: Organometallic compounds- Organometallic compounds that consists of bond between carbon and metal…

Q: Show how to synthesize the following product as the major product using any reactants/reagents and…

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Q: From compounds of 4 carbons or less and any reagents you want; synthesize the following compound.

A: Terminal alkynes has acidic hydrogen and hence when we treated with strong base and alkyl halide to…

Q: Devise a synthesis for below product from the given starting material. More than one step is…

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Q: What starting materials are needed to synthesize each compound by a crossed Claisen reaction?

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Q: Select the major product of the following reaction. H+ ОНС. NH2 H20 major product

A: In acidic medium, amine group condensed by the Aldehyde group by removing water molecule and forming…

Q: Draw the products of each reaction. NBS NBS Br2 b. CH2=CH-CHg c. CH2=CH-CHa а. hv hv

A: In organic reaction when reactant reacts with different reagents to give different products. Every…

Q: What acetylide anion and epoxide are needed to synthesize each compound?

A:

Q: What reagent or reagents are needed to complete the following transformations? If more than one…

A: The conversion of the reactants to products are given below,

Q: h) Draw a stepwise mechanism for the following reaction. OH N° NH,OH MEOH

A: The reaction in which intramolecular transfer of proton is known as tautomerism.

Q: Devise a synthesis of each compound from cyclopentane and any other required organic or inorganic…

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

Q: Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts. Br…

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Q: Draw the products of each reaction.

A: (a) The reaction of alkene with N-bromosuccinimide in presence of light results in the formation of…

Q: Devise a synthesis of each product from the given starting material. More than one step is required.

A: Since your question has multiple subparts, we will solve only first three sub parts for you. If you…

Q: ES Draw a stepwise mechanism for each reaction. Br NaOH a. Br NH2 + H,0 + Na8r NABH4 + H,0 CH3OH NH2…

A: The answer to the following question is-

Q: CN

A: We have to convert the above reaction

Q: SH

A:

Q: Draw a stepwise mechanism for the following reaction.

A: 1.protonation of an alcoholic group in the presence of acid HBr Removal of water for the formation…

Q: Indicate how the following compound can be synthesized from the given starting material and any…

A: The given compound can be synthesized using following steps from the given starting material :

Q: Predict the major product or reagent that completes the transformation

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Q: Devise a synthesis for each compound, starting with methylenecyclohexane and any other reagents you…

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Q: Draw

A: This reaction is called Wittig Reaction because Ketone Carbonyl compound react with phosphoylide.

Q: (def) Predict the major product or reagent that completes the transformation

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: Draw the products of the following reactions w given starting material 4. NaNH2 followed by CH3CH2Br…

A: When alkene is treated with sodium amide , removal of proton takes place. When this treated with…

Q: When a cyclic ketone reacts with diazomethane, the next larger cyclic ketone is formed. This is…

A: To draw a mechanism for the below ring-expansion reaction.

Q: Draw a mechanism for the following transformation: OH ď H₂O [H+]

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Q: Propose a synthetic route to the indicated product: ÓH

A: -COCH3 group is electron withdrawing group.  Thus it is meta directing group for electrophilic…

Q: Draw a stepwise, detailed mechanism for each reaction.

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Q: Show how pent-2-yne can be made from two different alkyl bromides using two necleophilic…

A: The preparation of alkyl halides can be done using various preparatory methods. In case of…

Q: NABH4 CH3OH + H,O NH2 Draw the product of each step. NH2 draw structure .. proton transfer

A: Applying concept of reduction followed by proton transfer and cyclisation reaction.

Q: Synthesize the following synthesis starting from the starting compounds using the necessary organic…

A: Given conversion is : Complete the following conversion = ?

Q: Propose a synthesis using the given starting material and any other reactants or reagents. Do not…

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Q: Draw the major product of each reaction. 1) Hg (Oac ) 2 4 2) Br₂ / H₂0 3) NaBHy 03 H₂/Pd m PCBA H₂0²…

A: Given:  To find: the major product when the given compound(vinly cyclohexane) reacts with the…

Q: Draw the product of each reaction.

A: To find: The product of the given reactions

Q: Please draw thesthe of 2-methyl-2-hexene from a carbonyl and an phosphonium ylide

A: The reaction of carbonyl group with phosphonium ylide produces an alkene. This reaction is mainly…

Q: 3) Propose a multistep synthesis for the following transformation. Draw all reagents necessary for…

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Q: A B,Y-unsaturated carbonyl compound rearranges to a more stable conjugated a,ß-unsaturated compound…

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Which compound is the major product of the reaction sequence shown? (1) SOC2 (A) (B) HO. (2)…

A: Given is two step reaction.

Q: Draw the enol form of each keto tautomer in parts (a) and (b), and the keto form of each enol…

A: Keto-Enol tautomerism is an equilibrium that exist between carbonyl group (aldehyde and ketone) and…

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

A: a.

Q: Draw the major product of this reaction. Ignore inorganic byproducts. CN 1. DİBAL-H 2. H3O* Select…

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Q: b. C. Br

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Q: Devise a synthesis of each compound from cyclohexene and anyrequired organic compounds or inorganic…

A: Given:

Q: 3. Propose a synthesis of the following from the given starting material and any other reagents 2.…

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Q: Draw the major product of each of the following reactions:

A: epoxide ring-opening reaction is a base-catalyzed reaction. in this reaction, the hydroxide ion on…

Q: Be sure to answer all parts. Be sure to include the ion charges. Draw the products of each acid-base…

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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.