alkali `CHO H3O*

Q: Suggest short, efficient reaction sequences suitable to produce the compound from the given starting…

A: We have to carry out the required transformation.

Q: 2.

A:

Q: Give the major product (16) and the mechanism for the elimination reaction given below.

A: In this question, we will draw the major product with mechanism and explanation.  You can see the…

Q: Provide the full mechanism for nitration of benzene. Show how the electrophile is formed and how the…

A:

Q: DMSO 0

A:

Q: (a) Give mechanism of preparation of ethoxy ethane from ethanol.(b) How is toluene obtained from…

A:

Q: Rank the indicated hydrogen atoms in order of increasing ease of abstraction in a radical…

A: The ease of abstraction of hydrogen in a radical halogenation reaction depends on the stability of…

Q: Define the Reaction of Organometallic Reagents with Other Compounds ?

A: The compounds containing bond between carbon and a metal are termed as organometallic compound.

Q: Show how the Suzuki and/or Heck reactions can be used to prepare the following compounds:

A: The Heck and Suzuki reactions are used for the generation of new Carbon-Carbon bond. These are…

Q: Give the structure of the major product of the following reaction. Explain why you think it is the…

A:

Q: MgBr O CI 2) H30* pyridine

A: See mechanism  below.

Q: B3. Write a detailed mechanism for the following Knorr Synthesis 1) (BUO-NO (0.5 equiv) , HCI A…

A: Preparation of pyrrole compound by using beta amino keto-ester and beta-keto ester is called Knorr…

Q: Suggest short, efficient reaction sequences suitable to produce the compound from the given starting…

A: Here we are required to synthesize the given compound

Q: provide appropriate product 9. Br 1. Pd Ln, EtsN, MECN, Me Me 2. MCPBA, CH2Cl2 3. НСЮ, ЕОН

A:

Q: The following compound can't be synthesized using the methods discussed in this chapter. Why not?

A: Introduction Why the compound shown (m nitrotoluene) cannot be prepared using the methods studied in…

Q: Suggest a mechanism for the following reaction. Explain why NaB(CN)H3 is preferable to NABH4 as…

A: We have to suggest mechanism for the following reaction in step 2

Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. H-A HN H20 H2N HO

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. OH LOME TSOH, H20 OMe

A:

Q: Give the products of, AND mechanisms of formation for, ALL reactions in BOTH synthetic schemes. OH…

A:

Q: In the reaction scheme below, the furan A is converted to the thiophene B via a diketone. Write a…

A: Formation of a Diketone:

Q: Give the major organic product for the reaction paying particular attention to regioselectivity. "D…

A: See major products below.

Q: Give the major product(s) of the following reaction. Mg Br

A: This reaction shows the formation of very important reagent in organic chemistry that is grignard…

Q: Which of these reagents is used in the Clemmensen reduction?

A: Clemmensen reduction = reduction of aldehyde or ketone to the corresponding alkane.

Q: Outline two different ways that butan-2-one can be prepared from a nitrile and a Grignard reagent.

A: The reaction of the Grignard reagent with a nitrile compound gives imine which on hydrolysis…

Q: Drag and drop the synthetic steps provided in order to propose a reasonable stepwise preparation of…

A: Given compound is :

Q: The mechanism by which the haloform reaction works. Explain.

A: We have to give the mechanism of haloform reaction.

Q: Give the following synthetic transformation of this reaction of silicon chemistry: NH₂ OMe (i)…

A:

Q: Show how the Suzuki and/or Heck reactions can be used to prepare the following compounds:

A: Suzuki reaction: A reaction that couples an aryl halide or vinyl halide with an organoboron reagent.…

Q: Explain why the following substrates cannot exhibit Friedel and Crafts reactions.

A: Friedel-Crafts Alkylation is the reaction of benzene with alkyl halide in the presence of a Lewis…

Q: to write ionic equation for the reaction of acetic acid with itheim bromide, and specify Rwhether…

A: Starting materials Acetic acid : CH3COOH Lithium bromide : LiBr   pKa of acetic acid = 4.7  pKa of…

Q: Give the major organic product for each of the reactions

A: To solve this problem we have to give the major products formed by the given reaction .

Q: Give the mechanism (arrow-pushing) for the reaction below. NAOME/MEOH \Br b. Name the product of the…

A: The mechanism is provided below:

Q: Give the structure of the major product (s) for the reaction listed below:

A:

Q: AICI3

A: It is an example of Friedel craft acylation reaction, Here a new cyclic ketone formed as the major…

Q: Give the structures of A and B in the following reactions. Pay special attention to stereochemistry.…

A: m-CPBA (meta chloro per benzoic acid)--->> It is used for epoxidation of alkene and also used…

Q: What is the major product is expected in the following reaction

A: Given : We have to make the major product for the following reaction.

Q: The following reactions produce one major organic product. Give the product of each reaction. NBS…

A: N-Bromosuccinimide or NBS is a chemical reagent used in radical substitution, electrophilic…

Q: 3. Provide the major organic product of the following EAS Reaction.

A: Given : structure of reactant EAS reaction happens according to activating group.

Q: 4. ŽI 3.

A: The answer is as follows:

Q: Provide detailed reaction mechanism and reagents required for the synthesis of B from А. Br A

A: Grignard reagent is prepared by inserting mg metal in the between carbon and halogen.

Q: What is the expected percentage of the major product in monobromination reaction?

A: If X= cl then I calculate  Persontage of products

Q: Complete the Reaction below and provide the following (i) a detailed stepwise mechanism to account…

A:

Q: provide the mechamism and tell the name of each reaction d. КОН / Н20 е. 2 ~OH H30*

A: d. Aldol condensation:The alpha hydrogen of carbonyl compounds is acidic in nature and it is removed…

Q: H,Cro, CH, NH, H+ NABH,CN -он -H NABH, но H- -он HO, CH,OH H H,C.

A:

Q: Which of the following will give a positive Jones test? (i.e. Which will undergo an oxidation…

A: Jones test is a test for such functional group which can oxidized by Jones reagent.

Q: Provide all resonance structures of the sigma complex when aniline reacts with an electrophile to…

A: Reaction is taking place between aniline and Br2 (Br electrophile)

Q: Give the minor product of the following reaction. ? heat CHO CHO There is no reaction under these…

A: the correct option is B. hence the minor product is B.  the option b the repulsion is more then…

Q: Draw the structure of the major organic product in the following hydroboration-oxidation reaction.…

A: Hydroboration–oxidation reaction: The hydroboration–oxidation reaction is a stereospecific two-step…