Qs.1 Complete the following reaction. Show mechanism. What is the specific name of this reaction? Can it be done under basic catalysis? OH H3O* + HO.

Q: Show the organic product formed when 4-methylpentanal is heated with sodium methoxide in methanol as…

A: We will find out the reaction product

Q: Show the product of the following reaction. nucleophilic carbene catalyst

A: The terminal alkenes present at C-13 and C-1 on the same molecule, leading to an intramolecular…

Q: Perform a retrosynthetic analysis of the following target and come up with the synthetic route. OEt…

A: There are number of functional group associated with organic compounds which impart specific…

Q: OH

A: 1. This reaction is in thermodynamic equilibrium state.  2. Here products and reactants are in…

Q: finish the retrosynthesis of the following   Starting with ethyne, how can you make 2-bromopentane…

A:

Q: The following is an aldol condensation reaction which involves two different carbonyl compounds, one…

A: The answer to this question is given below:

Q: Provide the mechanism and the product for the following reaction. (HINT – pyridine is a Brønsted…

A: In organic chemistry, the reaction can proceed via several pathways. The four major reaction…

Q: CN Br Na CN NaOH CN NaOH COOH Valproic acid

A: The solution is given below -

Q: CH2=CHCH,CH2CH3

A: Given-> CH2=CHCH2CH2CH3

Q: Complete the mechanism for the reaction of butanone with NABH, followed by the addition of aqueous…

A: When a ketone is reduced with sodium borohydride and acidic hydrolysis, then ketone is changed into…

Q: Exl. OH Ph ) Ho A Ph KH,18-c-4, THF, (i) 2) NO2 Xylanes, hat NO2

A:

Q: a) но н sock pyridine h)

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

Q: Show the mechanism and products formed when the given molecule reacts with NaOD and D2O.

A: When D2O is added in the reaction, the deuterium atom substitutes the proton of hydroxyl group. The…

Q: Treating PGC2 with a strong base such as sodium tert-butoxide followed by addition of acid converts…

A: A mechanism for the reaction of PGC2 to PGA2 has to be proposed.

Q: Give the major product of the following reaction. MeO H2

A: Given,

Q: Show the organic product formed when methyl propanoate is reacted with lithium diisopropyl amide,…

A: ester in presence of base form enolate and carry out cross clasisen condensation with other ester.

Q: Complete the following retrosynthetic analysis. Supply all reagents and precursors. Parts A and B…

A: Detail forward synthesis is given below along with retrosynthetic pathway

Q: In order to synthesis 1-phenylbutan-1-ol, you started the reaction with a hydration of prop-1-ene…

A:

Q: Drag and drop the appropriate reaction conditions over each arrow as appropriate. Keep in mind the…

A:

Q: Complete the following retrosynthetic analysis (the final product is shown first, and the initial…

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Q: The first reaction below gave a mixture of isomeric products A and A'; treatment of the mixture with…

A:

Q: Show the product and arrow pushing mechanism for the following reaction. Make sure that label the…

A: The product of the given organic reaction is as follows.

Q: B. Using curved arrows, show the mechanism for the formation of A-1 haloalkane through electrophilic…

A: Formation of haloalkane:

Q: Show the synthesis for the following Reactions. M Ô olt Nit2 Br -NH₂

A: Please find the attachment

Q: Show the mechanisms for the following reactions. Show all movement of the electrons. Do not skip or…

A: The first reaction is the addition of DCl to 2,4-Hexadiene. The first step involves in the reaction…

Q: S) Show the steps necessary to make 4-methylhexanoic acid using a malonic ester synthesis.

A: To synthesis a Product 4-methylhexanoic acid usic malonic ester as starting material ....

Q: Show retro-synthetic analysis leading from the target molecule to the precursor molecule showing all…

A: Given:- We have to transform the synthesis of given following below:

Q: a) Show how to make the following ether starting from Propylchloride and 2-lodopropane, keep in mind…

A: The given ether can be synthesized by carrying out Williamson's Ether synthesis.  It is a SN2…

Q: Show the reaction mechanism of 2-butanone with the appropriate reagents to obtain an enamine.

A:

Q: This reaction shows that an aldol-type reaction can be performed with a deprotonated imine as the…

A: Aldol-type reaction: The reaction in which enolate form of aldehyde or ketone reacts with α Carbon…

Q: While your aldol reaction was running, your TA announced that the the sodium hydroxide solution…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Kindly show the mechanism when you synthesize 2-hydroxypropanoic acid from ethanol

A: We have to show mechanism

Q: Qs3. Show how to synthetize the following B-keto ester from corresponding esters (show structures of…

A: The given is a beta keto-ester which can be formed by Claisen condensation of esters, which is when…

Q: Use retrosynthesis analysis, to get synthons and synthetic equivalents to show how to prepare the…

A: Answer is explained below. The synthons and the synthetic equivalents are as follows:

Q: Show the retrosynthesis mechanism of this equation with curved arrows representing electron transfer…

A: Note : 1-Butene on hydroboration and oxidation produces the 1-butanol. Benzoic acid and 1-butanol…

Q: Please show me the mechanism for O3+2-methyl-2-butene, stoping at the ozonide?

A: Ozonolysis is an organic reaction in which ozone is reacting with unsaturated compounds such as…

Q: Show the mechanism of the nucleophilic addition reaction of an alcohol with an isocyanate to yield a…

A:

Q: QUESTION 3 Show how you would synthesize the epoxide starting from cyclohexanol and benzyl alcohol…

A: We have to carry out the given synthesis. Consept: Step 1: In the step cyclohexanol is converted…

Q: Provide the mechanism and the product for the following reaction. (HINT – pyridine is a Brønsted…

A: The given reaction undergoes from cyclic ester to cyclic amide with the help of given reagents.

Q: On your answer sheet below the answers to the prior problems, draw the major organic product(s) of…

A:

Q: Show the mechanism and products for the reaction of 2-methyl-2-hydroxypropane + methanol.

A: In first step, methanol has acidic proton hydrogen bonded to oxygen, so H of -OH in…

Q: Show the retrosynthesis and the synthesis of the following compounds: OH Target material Starting…

A: Dear student, the given question is a multiple question, hence I solved first question according to…

Q: CH3 CH3 from OH and isopropyl alcohol

A:

Q: a) Provide the complete mechanism for the following reaction. Meo CH;CH2NH2 CH;OH b) Design a…

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Q: Propose a synthetic method to hydrate but-1-ene, which will yield the product opposite of 2-butanol

A: The reaction considered is the hydration of but-1-ene, a terminal alkene.

Q: estion: please show the mechanism for the formation of an alkene using the Wittig reaction for this…

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Q: HO.

A:

Q: Provide the mechanism for the 2nd reaction in this synthesis: D2S04 PSO4

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Q: 2. Identity the reagent sequence in the following transformations (retrosynthesis). A. OH B. он

A: These conversions can be done with the help of grignard Reagents and substitution  reaction.