reagents in the correct order for the synthesis of the target molecule?

Q: Design a synthesis for the target molecule from the indicated starting material.

A: In the synthesis reaction, we will be using following steps. 1) Reacting the initial reaction with…

Q: With an example describe mechanistically how an extraction is carried out acid-base.

A: Acid-base extraction is employed to separate acidic and basic compounds from a mixture.

Q: a) b) HO, HO c) OH Br

A: The cyclohexanecarbaldehyde will firstly reduce to alcohol via a reducing agent. The reducing agent…

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: Provide a multi-step synthesis to create the intended product for the listed original reactant. The…

A:

Q: Provide the reagents necessary to complete the following synthesis. Upload your synthetic…

A: 1. Ketal deprotection. 2. Grignard addition. 3. oxidation. 4. Wittig reaction. 5. Epoxidation. 6.…

Q: Describe how the target molecule (butanone) can be synthesized in a high yield from butane.

A: The given final product is a ketone named butanone and the starting compound is an alkane. So when…

Q: Chemistry complete the synthesis mechanism, show each step H,N

A:

Q: Provide the mechanism for the 2nd reaction in this synthesis: D20 o-k

A: This can be explain with the help of chair for. In the product the D group is present on the dash ,…

Q: Please help me solve this synthesis. It takes 5 steps

A: OKAY, I will give complete synthesis by using 5 steps.  You can see step by step solution. How to…

Q: 10.Draw the structure of the product of the reagent(s) with the substrate: SOCI,

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: NO2 Br

A: The conversion is given below in pic.

Q: Ethane

A: We have to propose a synthesis from ethane to butan-2-one. The required synthesis is shown below

Q: What steps use in the Robinson Annulation?

A: Robinson Annulation is an organic reaction, in which the reaction between methyl vinyl ketones and…

Q: Using retrosynthetic analysis, design a synthesis of the following target. HO Br Target

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Which routes could be used to synthetize the product in the center?

A: We have given the product in the center which is an organic compound names as alchol. We have given…

Q: OH (TM) (CH₂)4CH3 (SM) H

A: Here we have to synthesize the following given target compound from the given starting material by…

Q: Starting material multi-step synthesis?

A: The synthesis given is,

Q: alkenes possessing five carbons or fewer. OEt ethyl acetoacetate or EtO OEt diethyl malonate and…

A:

Q: 6 Show how to synthetize the following target: (a)

A: Organic reaction mechanisms.

Q: он но

A: We can begin the conversion from the elimination reaction of the alcohol to give an alkene.  The…

Q: Q. Can anyone please show me the details steps involved in the retrosynthesis of the target…

A:

Q: OH HO CH3

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

Q: From the below reactions, indicate which product is the Markovnikov product and which product is the…

A:

Q: Based on the image attached, explain the step-by-step mechanism reaction of nitration for methyl…

A: Nitration is carried out by concentrated HNO3 and H2SO4 mixture.  HNO3 + H2SO4 = NO2+ + H2O + H2SO4…

Q: TM H Show the synthetic sequence that converts acetylene to the target molecule (TM) shown below.

A:

Q: The reaction below is homogenic homolysis heterolysis heterogenic

A:

Q: Which of the following represent the reagents in the correct order for the synthesis of the target…

A: The first step in the reaction is known as Friedal craft acylation in which arenes are treated with…

Q: Design a synthesis to accomplish the following in two or more steps. steps Bno.

A: 1. Reduction of Lactone with DIBAL-H.2. Condensation reaction of H2H(n-Pr) with the aldehyde.3.…

Q: 8. Design a synthesis of the target molecule from the starting material shown. ОН "ОН

A: The given tertiary butyl alcohol reacts with conc. Sulfuric acid and gives 2-methylpropane.  It…

Q: product of Dehydration using sulfiric acid

A: Given compound is a secondary alcohol, which give dehydration Reaction in presence of sulfuric acid.…

Q: Draw the product of the attached reaction:

A: Product of the above reaction is given below,

Q: Provide a synthesis of the following target from the given starting material. from OH

A: The carboxylic acid can be first converted to the shown compound as follows:

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

A: Please find the attachment

Q: Select the best set of reagents for carrying out the following synthesis

A:

Q: Why is the following reaction sequence not an efficient approach to the desired product?

A: terminal alkynes contains acidic hydrogens  eg: acetylene (ethyne), 1-propyne etc this acidic H…

Q: cyclopentene with HCl

A:

Q: 10. Use multiple steps to complete the synthesis below. ОН Br

A: Bromo alkane forms grignard reagent on reaction with Mg metal in dry ether medium.  Alkyl group of…

Q: + ČH3 azulene

A: Cyclopentadienyl anion acts as a nucleophile while N-methylpyridine as an electrophile. Reaction…

Q: What are the conditions needed in a synthesis to promote an SN1 type of reaction? For example do we…

A: SN1 reaction is a nucleophilic substitution reaction in which the rate determining step depends on…

Q: Can you assist with identifying starting donor and acceptor compounds are needed to form the…

A: In this question, we want to identify Donor and Acceptor in Michael Reaction.  You can see details…

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

A:

Q: 4. Give a short, efficient synthesis of the target compound from the indicated starting material and…

A: The required synthesis is as follows:

Q: What is one commonly used way to turn a poor leaving group into a good one?

A: Since you have posted multiple questions, we are entitled to answer the first only. Please repost…

Q: QUESTION 58 Show how the following synthesis could be carried out. More than one step is required.…

A: Reagents involved in the conversion are 1) E. NaH 2) D. CH3CH2CH2Br 3) B. H2O, H2SO4, HgSO4

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: Propose a synthesis of the following target compound starting from benzonitrile. Remember to start…

A: Benzonitrile is first fluorinated then reduced to give benzyl amine which was then alkylated.

Q: Explain Tautomerization with example?

A: Tautomerization

Q: In the reduction of carbonyl compounds with NaBH4, the nucleophile is ______.

A: Nucleophile is a negatively charged or electron rich species which attacks on the positively charged…