Suggest a retrosynthesis of product A shown below leading to the starting material B and provide the synthesis of the desired product You may use any other reagents you deem necessary detailed mechanism is required

Q: Show the reaction to obtain the given product starting from a suitable carbonyl compound.Also give…

A: Reduction of Organic Compounds leads to decrease in the number of carbon-hetero atom bonds or…

Q: CO,Et

A: Answer

Q: Provide the Cruved arrow mechanism of anisole treated with bromine with iron (III) bromide. Include…

A: Here we are required to predict the mechanism of anisole with bromine with FeBr3.

Q: Provide a plausible synthetic pathway for the following organic transformation starting with acetic…

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Q: Provide the missing reagents in the following multi-step synthesis.

A: The organic reaction is given with missing reagents and it is required to complete the reaction by…

Q: Suggest synthetic routes to each of the following form the indicated starting materials. You may use…

A: Here the reactant but-1-ene is converting to  3-hydroxy-octane through series of organic reaction…

Q: Synthesize the following compound via Claisen condensation and any other necessary reagent.

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Q: (a) Propose a mechanism for the following reaction: кон, н,о (b) What other product is formed?

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Q: Propose a mechanism for the following reaction and develop it

A: In this question we want to draw the mechanism for this transformation.  You can see details Step by…

Q: Propose a synthesis for each of the following compounds. (a) ОН (b) (c)

A: Given are organic reactions.

Q: Enones (a,B-unsaturated carbonyls) act as electrophiles. Consider the enone starting material given…

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Q: Propose a plausible and logical synthetic pathway for the following

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Q: provide a synthesis of

A: 1.  KMnO4 : It is strong oxidising agent , it can oxidise        1o alcohol into carboxylic acid…

Q: (a) он (b) (c)

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Q: CI ***** A Et Et Et B Et C Et Et D

A: ->In E2 elimination reaction antiperiplanar beta hydrogen eliminated and alkene formed.

Q: .give the mechanism of given bleow reaction with explanation

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Q: Provide a synthesis of that results in the two products shown, starting from the given starting…

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Q: Provide an example of each of the following including a full detailed mechanism:  Mixed Aldol …

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Q: Provide the retrosynthesis and a forward synthesis for the transformation from the starting material…

A: Synthesis: Step 1: Dehydrobromination using NaOEt. Step 2: Epoxidation using mCPBA. Step 3: Acid…

Q: Provide a synthesis of the following compounds using the given starting materials as your only…

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Q: Propose a predict the major product in each of the following reactions

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Q: please help with this question. thank you. Propose an efficient synthesis of for each of the…

A: 1. Alkenes upon ozonolysis to give carbonyl compounds , alpha hydrogen containing carbonyl…

Q: Give a clear explanation handwritten answer and give the mechanism of given bleow reaction and…

A: In this question we have to tell the product of the reaction.

Q: Represent the structures of intermediaries (A – C) and product D. Propose a mechanism for each of…

A: A molecular entity known as a reaction intermediate or an intermediate is created from the reactants…

Q: The following synthesis will no produce the product shown - explain what will happen instead

A: Concepts to be used: Lewis acid react with Lewis base preferably in friedel craft reaction.…

Q: Using the Malonester synthesis, write the synthesis of the following compound by showing its…

A: malonester synthesis is the chemical process in which the diethyl malonester is alkylated at the…

Q: Propose a synthesis for each of the following compounds. a ОН (b) (c) ()

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Q: Please synthesize problem B and D starting from benzene.

A: There are different types of electrophilic substitution reactions - 1- halogenation 2- nitration 3-…

Q: Но from

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

Q: Br

A: In organic synthesis, we convert one organic compound into another compound reaction it with…

Q: Rank the following carbonyls from the least to the most reactive towards a nucleophilic, provide a…

A: Aldehyde and ketone both combindly called carbonyl compounds In carbonyl group , carbonyl carbon…

Q: Please give the appropriate reagents to complete the following synthesis.

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Q: Use the EAA or DEM synthesis and show how you would prepare each of

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Q: Draw the structure of A and B and show the mechanism for the following reaction. Write all the…

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Q: Propose mechanism consistent with the following reactions a and b.

A: Since we know that HBr react with alkene in presence of peroxide by radical mechanism and follow…

Q: Can you show mechanism of an example of grignard reagent with epoxies and H3O+ and the various…

A: Solution:-  In Epoxides reaction with Grignard reagents to form alcohols The nucleophilic attack of…

Q: ce

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

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Q: SYN) Suggest how you would carry out the synthesisshown here using any reagents necessary. Hint:…

A: Grignard reagent contains an alkyl group attached to Mg. The alkyl group acts as a nucleophile.

Q: Show how you would synthesize the following derivatives from appropriate carbonyl compounds. (b) (c)

A: The carbonyl compounds on treatment with amines forms Schiffs bases.

Q: Propose a plausible synthesis for each of the transformation

A: Above organic compound can be synthesized by using following reactions; 1) treatment of terminal…

Q: (SYN) Suggest how you would synthesize each of the following from phenylethanone (acetophenone),…

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Q: Provide all reagents and solvents as well as any additional organic substrate necessary to perform…

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Q: Draw the major organic product for the following two-step reaction and state which enolate is…

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Q: Propose a forward synthesis for one of the two sequences below using whatever reagents necessary. Do…

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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.