rottamatenCNT quon ianobion HO smeotol oealt on mokest s yligns t Propose a way to carry out the synthesis below. hace

Q: (c) HO.

A: The synthesis of the target molecule starting from the given starting material is proposed below.

Q: An a,ß-unsaturated carbonyl compound can be prepared by a reaction known as a…

A: LDA is used to abstract the ‘H’ from the less hindered side to form the carbanion. Since both the…

Q: Propose a synthesis to convert borneol to isoborneol. Use as many steps as needed. ? OH OH

A: The given molecule borneol is a terpene derivative. To convert from borneol to isoborneol a two step…

Q: 5. The following aminoketone can undergo an intramolecular reductive amination. Draw the expected…

A:

Q: OH +

A:

Q: (d)

A: We can proceed this transformation on two simple steps. Let us try to draw these steps.

Q: The following three derivatives of succinimide are anticonvulsants and have found use in the…

A:

Q: Propose a stepwise mechanism for the following transformation. Me Me Me но Me SOCI2 CI

A: Given conversion,

Q: Devise 9 SynTas for the following L reactions acetamimophen.

A: When cyclic ester is heated with methyl amine , the ring open of this ester and gives amide,…

Q: O Two aldohexoses x and Y produce idintical osazone. Yow nitric aid ozidation gives an optically…

A: Now, if we get a D- threose on two successive Ruff degradation of Y, then Y have have two more…

Q: propose a plausible synthesis

A:

Q: Show haw struclure A. youo are able to gek stecture B fam CEN Hint There are 5 Steps AA • A+…

A: Para-chloroenzenenitrile in presence of H+/H2O gives amide

Q: 3. Provide a mechanism for the following: acetyl CaA COASH co a. b.

A: 1. In presence of acid,  esterification occurs when carboxylic acid and alcohol reacts. 2. In…

Q: NO2 COOH

A:

Q: Provide mechanisms and/or products for the following transformation. Me 'N' Me (.5 equiv) H „CHO Me.…

A: Step 1: Acid catalyzed enamine synthesis followed by Diels Alder reaction ( see below).

Q: nthesis, show two different synthesis strategies. In the first synthesis strategy, include e…

A: The questions based on organic reactions. We have to convert the reactant into product by a series…

Q: Show a reasonable mechanism for the following reaction (Hint: Michael addition followed by…

A:

Q: Identify A in the attached reaction sequence, and draw a mechanism forthe conversion of A to B. B…

A: The Sharpless asymmetric epoxidation involves the reaction of allylic alcohols with the titanium…

Q: Page fropase an efficient synthesisto.comvert the aformentioneolmimoryamine.into Lithe tertiany mne…

A:

Q: ouer give the major produt of thisradica reaction.? 유 AIBN Product? Ph Ph HSn Bu By

A:

Q: Propose a mechanism for the following transformation: Et Me он 1) Excess EtMgBr 2) H30* Me "CI 'Et

A: Three membered rings formed by two carbon and one oxygen atom is known as an epoxide ring. The…

Q: Provide the reagents necessary to synthesize the following molecule. Ph > Me Me

A:

Q: The following reaction occurs through an Elcb mechanism followed by a tautomerization. Provide a…

A: E1CB is a two step reaction in which the intermediate formed is a carbanion and is one of the…

Q: React the substrate with excess CH3MgBr in ether, followed by subsequent water work-up. O O

A:

Q: 2. a. Provide mechanisms and/or products for the following transformation. Me Me (.5 equiv) H NET2…

A: Reaction 1 : Acid catalyzed enamine synthesis followed by Diels Alder reaction.

Q: Show how to synthesize the following compound  using either the malonic ester synthesis or the…

A: We can use the malonic ester synthesis pathway to get Cyclobutyl methyl ketone. The synthesis…

Q: 21) Propose a mechanism for the following reaction. OH H2O, H*

A: Alkenes undergo addition reactions in presence of water and acid. The reaction proceeds via the…

Q: b. Suggest mechanism for synthesis of the following cyclic ester. OH CO, Bu,N Pd(OAc),

A: Ans

Q: Propose a multi-step synthesis pathway that utilize the indicated substrates to synthesize the…

A: sequence:- free radical bromination nucleophilic substitution

Q: Propose a two-step synthesis for the following transformation. ? HO

A: Alcohols undergo dehydration to form ether. The reaction takes place via SN2 mechanism.

Q: Complete the following synthesis with the missing reagent(s) or major product(s). OH MCPBA OH CN…

A: Here we have to write the reactant, reagent and products-

Q: 4. Propose a multistep synthesis for each of the following transformations: a) CN HO. b) Ph OTs

A:

Q: Butacetin is an analgesic (pain-killing) agent that is synthesized com- mercially from…

A: The structure of p-Fluoronitrobenzene is; Butacetin is synthesized from p-Fluoronitrobenzene.

Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With…

A: SOCl2 reagent is used to convert acid into halide. This is one of the preferred pathway because the…

Q: 2. a. Provide mechanisms and/or products for the following transformation. NEt2 „CHO Me Me (.5…

A: Reaction 1 : Acid catalyzed enamine synthesis followed by Diels Alder reaction. ( see below).

Q: no-H Glycosylated Brat, on on n- OH on B Valy BH BH/B -> Braw arrow pushing de protonations…

A: To write the arrow pushing mechanism:

Q: An imine is hydrolyzed under acidic conditions. NH H20 + NH3 (18-20) Draw the complete mechanism for…

A:

Q: Predict the product of the following sequence: A A в в с с D D Me NET₂ Me Me 1. LDA, THF; Mel 2.…

A: Since LDA is a strong base, it deprotonates at the α-position to the ketone group to form enolate.…

Q: CH2CH3 HO,

A: In this question, we want to Synthesized the final product from the starting material (…

Q: 25. Provide the reagents necessary for the following transformation. OH ??? CI А. SOCI2, pyridine В.…

A: To find: reagent used to transform 2-methylhexan-2-ol to 2-chloro-2-methylhexane.

Q: OH

A: In this question, we want to Synthesized the final product by using the starting material and…

Q: Show experimental conditions by which to carry out the following synthesis. MeOOC Ph CHO + OMe Ph…

A: The experimental conditions by which the given synthesis occurs has to be given.

Q: (b) Visualise the retrosynthesis for the (as following instructed) (i) (ti) PH target compounds…

A:

Q: MeO Me N Propose a synthesis for the following transformations.

A: The question is based on the concept of organic reactions. we have to convert the given Reactant to…

Q: Propose a synthesis for the following transformation. OEt H' HO,

A:

Q: 12) Show how the following synthesis can be carried out: СН3CH2CHCH3 from HCECH Br

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…