HNO3 Zn A B D H2SO4 HCI or

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

A: enolate attacks the carbonyl electrophile and forms enone  Generally this is resembles to aldol…

Q: e a short note on how to perform the Acree-Rosenheim reaction test. Make sure to mention the…

A: The Acree-Rosenheim test is performed in the chemical laboratory. Generally, the active reagent for…

Q: Why aryl bromide is a bad starting material for an electrophilic aromatic substitution? What is…

A: For electrophilic aromatic substitution ,the phenyl ring should be electronically enriched as…

Q: What would a possible synthetic route for the following reaction be?

A: To obtain the desired product we have to prepare vic.dihalide in cis position then reaction of this…

Q: Which solvent would have a higher reaction rate for SN1? acetone ethanol Why does the solvent you…

A: Ethanol is a polar solvent that is used in SN1 reactions.

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

A: Given compound is :

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: How does doubling [B:] affect the rate of an E1 reaction?

A: E1 reactions are the unimolecular elimination reaction. This is a two step elimination reaction, in…

Q: If a large excess of the nitrating reagent is added, does the product produced contain one nitro…

A: Given: Excess of Nitrating mixture To find: Product will have one nitro group or more than one nitro…

Q: Br Br or

A:

Q: Which benzylic halide reacts faster in an SN1 reaction? Explain.

A: The explantion for the classification stated above is as follows :

Q: a. Explain why 1-bromo-2,2-dimethylpropane has difficulty undergoing both SN2 and SN1 reactions. b.…

A:

Q: Draw the starting material that would be needed to make this product through an intramolecular…

A:

Q: ore Br

A:

Q: Which solvents are preferred for an SN2 reaction. Why is this? Which solvents are preferred for an…

A: SN2 means substitution nucleophilic bimoleculer reaction. In this mechanism, bond breaking and bond…

Q: Why doesn't iodoethane react via Sn2 with NaI in acetone? It is a good leaving group and it is on a…

A: 1 .Nature Of Solvent Solvent SN1 SN2 Polar Aprotic Solvent (Acetone)   SN2 will favor Polar…

Q: A nucleophilic addition is not considered SN1 or SN2 because: A.) The reaction proceeds through an…

A: Given, Nucleophilic addition is not considered as SN1 or SN2. Why? SN1 stands for unimolecular…

Q: Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol…

A: Aldol reaction is an addition reaction occurs in aldehydes and ketones. Aldol reaction is a…

Q: Draw the benzoic acid structure and explain which products will be formed as a result of the…

A: Benzoic acid is an aromatic compound (carboxyl group attached to benzene ring) and aromatic…

Q: Why does increasing alkyl substitution increase the rate of an E2 reaction?

A: The increase in E2 reaction rate with increasing alkyl substitution can be rationalized in terms of…

Q: Explain why a Lewis acid is necessary in this aldol reaction. Include a structure formed by the…

A: Lewis  acid  Facilitate  the attacking of nucleophile  to the carbonyl  carbon

Q: Why does bromination give exclusively anti products while chlorination gives a mixture of syn and…

A: Halogenation is the addition of halogens to alkenes. Halogenation usually gives anti products. If…

Q: Which one favors E2 reaction? A) isopropoxide ion B) tert-butoxide ion C) ethoxide ion D)…

A:

Q: BrMg. 1. 1 CI CI starting point 2. H3O* compound A

A:

Q: Rank the following alkyl halides in order of increasing reactivity in E2 elimination. Then do the…

A: Generally the increasing order of the alkyl halide in E1 and E2 elimination reaction will be methyl…

Q: Which types of halide will react faster in an SN1 reaction?

A:

Q: How do you explain why in base-catalyzed halogenation of acetone, the second (and third)…

A: Explanation: Base-catalyzed halogenation of acetone occurs through enolate formation. After the 1st…

Q: Using resonance structures, explain why a nitroso group (– NO) is an ortho, para director that…

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: write or draw the synthetic step to get to the following compounds. (Grignard reaction)

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

Q: All are true or false   a) The initially formed b-hydroxy carbonyl compound loses water in a Aldol…

A: a) The initially formed b-hydroxy carbonyl compound loses water in a Aldol condensation. TRUE- In…

Q: 14. Outline a synthetic route for converting A into B. This will require several reaction steps.…

A: Given is organic reaction.

Q: Perform a retrosynthetic analysis (please include - disconnection etc) and suggest a synthesis of…

A: The retrosynthesis method is used to determine the starting material by the fragmentation of the…

Q: One possible side-reaction of this experiment is biphenyl, explain how it can be formed.  Here is…

A: The reaction given is, => bromobenzene →Magnesium Ph-MgBr+

Q: Rank the reactivity of the following compounds according to the SN2 reaction? Please explain why a)…

A: The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group…

Q: reagents

A: In Negishi cross coupling Reaction, Aryl halide or vinyl halide react with Organozinc to form…

Q: H

A: Applying concept of organic synthesis via wittig reaction and organometallic.

Q: OH • You do not have to consider stereochemistry. • Draw the enolate ion in its carbanion form. Draw…

A: Given reaction is aldol condensation.

Q: Select the member of each pair that undergoes SN1 solvolysis in aqueous ethanol more rapidly

A: Given:

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol…

A: The reaction mechanism for the synthesis of given aldol product is,

Q: Draw the product of the E2 reaction shown below. Ignore any inorganic byproducts. Br KOtBu Drawing…

A:

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Но РСС, СН-Clz

A:

Q: If the alkyl halide in each of these reactions was an alkyl chloride instead of the bromide, A. the…

A: Given,  If the alkyl halide in each of these reactions was an alkyl chloride instead of…

Q: A small base like KOtBu or LDA favors the Zaitsev product in an elimination reaction whereas a…

A: There is an empirical rule which determines the major and minor product . Saytzeff and Hoffmann…

Q: Rank the alkyl halides in attached group in order of increasing reactivity in an E2 reaction ?

A: The increase in the number of R groups increases the rate of E2 reaction. The increase in the number…

Q: How does the negative inductive effect (−I) of chlorine in the ortho position of the phenol, reduce…

A: