this synthesis have flaw. ellaborate why this synthesis is wrong and do the ncessary corrections

Q: HO HO.

A: Here we are required to predict the reagent for the following conversion

Q: an alke

A: Alkanes, alkenes and alkynes are simple hydrocarbon chains with no functional groups. The simplest…

Q: Draw a reasonable synthesis for this reaction

A:

Q: Draw the mjor product of both question with mechanism asap

A: Given structure of reactants.

Q: Show the formation of given product with mechanism.

A: Ethylene glycol is generally use for protection of ketone. Hydrolysis reaction in acid medium used…

Q: Need help. Please draw out mechanism on how to get the product.

A:

Q: (SYN) Which solvent-acetone or tert-butyl alcohol-would be better to use to carry out the reaction…

A: E1 reaction is a unimolecular elimination reaction, which involves the removal of an HX substituent…

Q: Orgo synthesis problem needs to be done!

A: The above synthesis is completed in several steps.

Q: Draw Reaction mechanism for ephedrine. Left one is the example for aspirin

A: Reaction mechanism for ephedrine:- There are many methods or ways of preparation for ephedrine.

Q: How can do this reaction please O perpose mechanism

A: We have to carry out the following transformation. Also we have to give the mechanism of this…

Q: In this organic synthesis, can you help me to figure out A and ? mo. OMe DMA OMe マ」

A:

Q: at product will result from the reaction shown? (Just mention the class of compound not the…

A:

Q: Bonus: What anion is a more reactive nucleophile? Why? Must draw a picture! VS.

A:

Q: Draw the complete, detailed mechanism for the reaction shown here. Will the product be optically…

A:

Q: Draw the curved arrow notation and the resulting organic product for the heterolysis of…

A: In heterolytic cleavage one species take away both bonding electrons from the other species.

Q: williamson

A: In Williamson etherification Synthesis reagent is used NaOH or NaH ( base ) and solvent is THF .…

Q: Mechanism of this reaction please!

A: Given enzymatic reaction is:

Q: Please give mechanism with name of all of compounds and product and all other steps

A: NaBH4 is mild reducing agent, as it is insoluble in non polar solvents, therefore alcoholic or…

Q: NH, но Br

A: The given compound contains an alcohol functional group and bromine substituent. In presence of…

Q: Perform the Synthesis of this.

A:

Q: Please help me. Someone know the synthetic rute and conditions?

A:

Q: What is/are the most acidic proton) in the moloecle below? Select the anneer where the most acidic…

A: Given: structure of molecule.  Acidity is directly proportional to the stability of Carbanion.

Q: Which can ot be used in the second step of the reaction sequence

A: Azide ion is a strong nucleophile (far better than amines) and will readily participate in…

Q: Draw the missing curved arrow notation to incidate how the carbocation in left box rearranges to the…

A:

Q: Explain synthetic event in React js

A: SyntheticEvent may be a cross-browser wrapper around browser’s native event. In React all of your…

Q: Show mechanism for Vinyl Acetate (product) using Wacker Process Start with Potassium…

A: The process which is used for preparation of aldehydes and ketones from alkene is known as Wacker’s…

Q: Draw all the detailed plausible mechanism and all relevant resonance structures of the reaction…

A:

Q: Draw the products of attached reaction by following the curved arrows.

A: The product of attached reaction is determined as shown below,

Q: Give me mechanism. Please explain each step!

A: Following is the polymerization reaction of the given alkene.

Q: e problem to get the product shown. CI AICI3

A: The question is based on the concept of electrophilic substitution reaction . We have to account for…

Q: please  give reaction and Mechanism for the preparation of given molecule. PLEASE MECHANISM

A: You can see how to make this molecule step by step with mechanism also.

Q: (c) Provide two different yet valid for the following retrosyntheses compound (with synthesis). off

A: Synthetic planning starts with the final product ( target molecule) , which is fixed and…

Q: What alkyne (or diyne) yields attached set of oxidative cleavage products?

A: alkyne (or diyne) yields attached set of oxidative cleavage products is

Q: True or false: Th application of the organometallic is depend on the metal type, if the M is main…

A: Given Th application of the organometallic is depend on the metal type, if the M ismain group use as…

Q: Explain why substitution is difficult on accomplish on the benzene ring?

A: Benzene is a planar molecule having delocalized electrons above and below the plane of ring. Hence,…

Q: ОН SAM Products ???? Mechanism????

A:

Q: Friefly explain why the following synthetic step is incorrect, and rewrite it so that it is correct.…

A: Need to correct the product for the given reactant.

Q: Can you draw the mechanism specifically for the cleavage part,

A:

Q: Draw the major product of this reaction. Ignore inorganic byproducts. H3O*, heat P Type here to…

A:

Q: Но 애 Lat

A:

Q: NaOH HzO エ の

A:

Q: (SYN) Show two different syntheses for the compound shown here, one using (CH3)2CULI as a reagent…

A:

Q: rmed for a split second before breaking into the products

A: When molecules of reactant cross the activation energy Barrier then these molecules form transition…

Q: complete

A: We will write the reaction conversion

Q: Draw a complete, detailed mechanism for the reaction CH3CH2OH shown here. H

A: Here the starting material is tetrahydropyran

Q: Draw the products of attached reaction by following the curved arrows.

A: The products of attached reaction by given the curved arrows can be drawn as

Q: practice problen ?

A: Please find the attachment.

Q: What is/are the reagent(s) for the following reaction? HO .. Problem viewing the image. Click…

A: In the given reaction primary alcohol to aldehyde formed. It oxidation reaction. Reaction so we need…

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.