Draw a complek, detailed mechanism AND predict the major organic producet for the follawmg trans formatins : Ca) NaOH Pynidmé oH (e) Hz Soy

Q: Indicate the reagent(s) needed to carry out the following transformations. a) он OTs b) но

A: NOTE : In the 2nd reaction, the H atom is present in the product attached to the carbon making…

Q: Me Me D Me Me + H* HN, A OH

A: Detail mechanistic pathway is given to find out the missing reagent and product

Q: 19) (1) Provide the majo Reduction, Clemme (A) Me2N (C) (E) (II) Provide the mechanism

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Q: Draw a stepwise mechanism for the following reaction, one step in the synthesis of the…

A: SOLUTION: Step 1: Pitavastatin (Livalo) is a lipid-lowering agent. It is used in the treatment of…

Q: Please explain the mechanism of the following reaction and explain why the epoxide is formed at that…

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Q: Q7. What carbonyl compounds would you reduce to obtain the folowing alcohoa CHyOH

A: Please note- As per our company guidelines we are supposed to answer only one question. Kindly…

Q: d) Explain why product C is racemic but product D fonned 12 mechinlsmwhin nesuts version of the…

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Q: Substitutions of Aromatic Heterocycles DMF POCI3 CH mecanssum mpletely altered by the presence of…

A: In a chemical reaction, the combination of two reactants in an appropriate molar ratio produces the…

Q: Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the…

A: The stepwise mechanism of the given reaction is shown below. 1. The formation of tertiary…

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: When reacted with methanol and an organic acid, dihydopyran yields one major product. Draw a…

A: Since the alkene is nuclophilic. Hence it takes the proton from the solution and form carbocation.…

Q: 2 Please wnte the Mechanism Par the reduchion of the acid Chloride Shawn belas to theCorcespalkn…

A: LiAlH4 is a reducing agent. It increases the concentration of hydride ions in the reaction which…

Q: Which reacton sequence will gve higher yds of the peproduc termedate Febr AIC ntermediate Febr AIC

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Q: One step in the synthesis of the nonsteroidal anti-inammatory drug rofecoxib (trade name Vioxx)…

A: Suzuki reaction is a type of coupling reaction. The product formed by the reaction is R-R. It…

Q: Determine the mechanism and draw the products of attached reaction. Include the stereochemistry at…

A: The given alkyl halide is a tertiary alkyl halide. The tertiary alkyl halide undergoes SN1 reaction…

Q: OTBDPS A Ph SnCl в OTES OTBS EtgAICI

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

Q: lycolysis: OP HO, 2-Phosphoglycerat- potol-(2PG)

A: Glycolysis is a bio chemical metabolic path way that converts glucose into pyruvic acid. The free…

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: (a) Draw the mechanism for the following transformation including reagents and any isolable species…

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Q: ai) Michaeladdition: which molecule is comrect Michael acc eqptor needed to create the prod.below? D…

A: We have to predict correct option for Michael acceptor.

Q: O usmg any othen Startng with acehe acid and necessang reagents, synthesize The following compornds…

A: 2 We have to synthesize the following given compounds by using any other necessary reagents starting…

Q: 9. Draw mechanism for all the substitution and elimination products for the following reaction.…

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Q: a) cuved amow nelation + draw mechanism include stereo, interrediates + final product, include lone…

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Q: Draw the structure of compounds A–E in the following reaction scheme.

A: The given reaction is shown below. In order to obtain the structure of all the compounds, the…

Q: In each of the following rea ctions, the indicated product is either obtained poor yretd all.…

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Q: 4) Lropose a synthetic route for the following rxn. Supply all necer reaguds s show the inter me…

A: The given compound is an amide. Amides react with an alkyl halide and CH3OH to give ester which…

Q: 4. det erMIne ene producu show Stepwise mechanism ant

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

Q: OCH3 D,SO4 + D20

A: The reactant given is an ether. Hence in the reaction, the O with lone pair electrons will take…

Q: j. 1,2-epoxybutane + acid in methanol Reaction Type(s) Mechanism(s) Product(s)_ Stereochemistry (if…

A: Answer-1  Reaction Type - Epoxide Opening in Acidic Condition  Answer-2  Reaction Type- Acid Base

Q: Provide the complete mechanism using Curved Arrow Formalism for the reaction of pyruvic acid…

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Q: Sue what reagents do I meed to symthesize this groduct from ithi'sre and what woud bethe…

A: We have to carry out the given transformation.

Q: 13. Draw the concerted mechanism for the following elimination. CH3O CI

A: In these reaction 2-chlorobutane react with strong base CH3O- to give but-2-ene. it follows…

Q: When fumarate reacts with D2O in the presence of the enzyme fumarase, only one isomer of the product…

A: Given reaction of fumarate with D2O in presence of enzyme fumarase is

Q: DBU OTs DMSO Me Ме Me

A: A question based on elimination reaction, which is to be accomplished.

Q: Comsider the Markomko 13btadene hoen net Wen thi is raded with HBe at 25"C the major product…

A: The given reactant is 1,3-butadiene. The addition of HBr to an alkene follows markovnikov's addition…

Q: (b) What happens when- (i) is fast treated with CH3 H3CCO,H and then the product obtained is treated…

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Q: Que- Pro posea two reaction sequenie to con vert each of the fallowing Subs trates in to the…

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Q: Circle the most probable mechanism vcle the mosr probalole mechanism C draw the produdfortue…

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Q: 1.70 An a,ß-unsaturated ketone reacts with a conjugated Wittig reagent to produce a relatively…

A: The wittig reaction is a chemical reaction for the formation of alkene from aldehyde or ketone with…

Q: Please select the appropriate reagent to complete the following transformations. A a B b C D | d…

A: The transformation taking place is given as,

Q: Identify the electrophilic site in the following molecule. C other than carbonyl O of carbonyl OC of…

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Q: CI- AICI3

A: Given,

Q: en the following optically active alcohol is treated with HBr, a racemic mixture nide is obtained.…

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Q: OsO4 H,S

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Q: have prosimately e same mas however. the veoaity (at room temperature).of Lanalin higher an the vwty…

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Q: Draw a reasonable mechanism to form the terpene shown from the biologičal precursors shown: Several…

A: First two substrate will undergo additive reaction followed by cyclization and hydration dehydration…

Q: Identify the intermediates (A–C) in the following reaction sequence, which was used to prepare…

A: Ofloxacin is an antibiotic useful for the treatment of a number of bacterial infections.…

Q: If the back- Side approachn (SNa) is hindered, the acetyiide 1on may abstraet a proton, gwing…

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Q: the nucliophile and of ing Heaction. Give a Meactions using cunved AMHOWS electmophile in each step…

A: Nucleophile is an electron rich species and electrophile is an electron deficient species.

Q: Identify the intermediates (A–C) in the following reaction sequence, which was used to prepare…

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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.