Show the electron-flow mechanism of amiline from benzoic acid, this involves predicting major and by-products using electronic and structural effects. The arrow push mechanism must be shown.

Q: Which is the organic product for the following reaction? KMnO4 H₂O

A: The alkyl group attached to the benzene ring having at least one hydrogen atom at the key atom can…

Q: Provide the structure (a single resonance contributor) of the key intermediate in the electrophilic…

A: The given reaction is an example of electrophilic aromatic substitution reaction.

Q: help please answer in text form with proper workings and explanation for each and every part and…

A: Here pyridine act as a base that abstracts the proton from the secondary amine to develop a negative…

Q: help please answer in text form with proper workings and explanation for each and every part and…

A: Part 2: Explanation:Step 1: Introduction to Hofmann Amine DegradationThe Hofmann amine degradation…

Q: Under the acidic extraction conditions with aqueous sulfuric acid, benzoic acid will be found…

A: We have an acid extraction with sulphuric acid , we have to see In what form benzoic acid will be…

Q: 20. What is the major product for the following reaction? EtONa, EtOH A) B) D) heat E) None of these…

A: -> EtONa is base which can abstract most acidic beta hydrogen to give alkene.-> EtONa is not a…

Q: Draw the structure(s) of the major organic product(s) for each of the following reactions. Br₂, A a)…

A: First example is a  bromination reaction in the formation of monobromo on the stable carbon of an…

Q: Identify the major and minor product(s) of the following reaction: Br NaOEt ?

A: Alkyl halide reacts with strong bases to produce alkenes as the major products.

Q: Which of the following reagents will convert an alcohol into a good leaving group? Mark all that…

A: The question is based on organic reactions.We need to identify the product and explain its…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

A: Carbonyl compounds are reactive due to the presence of  O=C group. They prefer to undergo…

Q: Synthesize the following molecule below starting from formaldehyde and alcohols of 4 carbons or less…

A: The given molecule is synthesized from formaldehyde and 4 carbon alcohol. The first step is the…

Q: Draw the organic product of the Lewis acid-base reaction shown below. Include all lone pairs and…

A: The given reaction is shown below.We have to draw the major organic product of this Lewis acid-base…

Q: What is the major product from the reaction shown? OH (A) H₂O -CH₂CH3 H

A: Alkene gives hydration reactions in presence of an acid catalyst. The reaction follows an…

Q: Perform the retrosynthesis (with their structures) and the synthetic route of these two molecules…

A: Given are organic compounds.Given compounds are diastereomers of each other. Compound 1 has trans…

Q: Predict the product for the reaction shown. ŞO3H IV H3O* A 11 © E III

A: Here desulphonation of  benzenesulphonic acid occur on heating  with H2O/H+ by electrophilic…

Q: Draw the starting reactant that would produce this alcohol when treated with

A: Given a reaction where:Product is a secondary alcohol (4-Heptanol)Reagents are: Sodium borohydride…

Q: Using the disconnection approach propose a reasonable retrosynthetic route to accomplish the…

A: The retrosynthetic analysis for the compound:

Q: Stan and Kyle have observed a reaction between the aniline derivative A and acetone. a) Stan…

A: The boy Stan likely to be more correct. Because when aniline reacts with the acetone it will first…

Q: on to react with the ketone in the remainder of the mechanism. The reaction takes placCe under…

A:

Q: Draw the product of this reaction. Ignore inorganic byproducts. Br Br 1. NaNH2, A 2. H3O+

A: The given geminal dibromide compound undergoes E2 elimination reaction when treated with strong base…

Q: Propose a mechanism for the following reaction that would yield the expected major product. SHOW ALL…

A: Given is organic reaction.The given reactant is tertiary alcohol.The given reagent is hydronium…

Q: 3. Starting from Anthranilic Acid show a synthetic route of preparing Isopropyl Anthranelate. You…

A: Isopropyl anthranilate is an ester which is produced by the reaction of carboxylic acid and alcohol…

Q: HBr

A: The main purpose of this question is to show the mechanism of bromination by using HBr reagent. The…

Q: Starting with cyclohexanol, give a sequence of laboratory reaction which could be used to produce…

A: Interpretation - Give a equence of laboratory reaction which could be used to produce cyclohexane…

Q: Draw the organic products of the reaction shown. Draw hydrogens on oxygen and nitrogen where…

A: When we react imines with HCl and water it forms carbonyl compound (aldehyde/ketone) and amines.…

Q: 1,2-Trans-cyclohexanediol has been shown to be an efficient support for the asymmetric…

A: PhLi can act as a nucleophile. It can undergo halogen exchange reaction to generate anion.

Q: 4. Provide the major organic product of the following reaction. Zn(Hg), HCl, H₂O

A: In this reduction reaction, ketones or aldehydes is converted into alkanes using zinc amalgam and…

Q: Prepare 2-methoxy-propanol from 1- bromo-propane. Show the steps and use any reagents you need.

A: The detailed explanation of this question is given below

Q: Provide the full reaction mechanism for the preparation of Aspirin (Not salicylate) starting from a…

A:

Q: Provide a synthesis of the target structure on the right from the starting structure on the left,…

A: The given synthesis scheme is shown below.We have to carry out the above synthesis.

Q: Which statements are true regarding the reaction of 1-chlorohexane with sodium ethoxide in ethanol?…

A: Here 1-chlorohexane reacts with sodium ethoxide in ethanol.

Q: What is the major neutral organic product for the following sequence? OH 1. POCIĄ pyridine 2. Os04…

A: An alcohol reacts with phosphorus oxychloride to give an alkene. This dehydration reaction occurs…

Q: Show how you would synthesize the following compound beginning with acetoacetic ester. 1589.0 logra

A: Given is organic compound.We can synthesize this compound by acetoacetic ester synthesis reactions.

Q: C For the mechanism step below, draw curved arrows to show electron reorganization. Arrow-pushing…

A:

Q: SUGGEST A REASONABLE synthetic strategy for synthesis of 4-methyl-1, 4-pentanediol from methyl-4-…

A: Esters reacts with Alkyl magnesium bromide (Grignard reagent) to give ketone. Ketone on further…

Q: How would you achieve the following transformations! AICI 3 COOH

A: Given that, the reaction conversion reaction is:

Q: Provide suitable strategy for obtaining NO2 from pyridine. Suggest mechanism.

A: To explain: the mechanism along with the reagents for the preparation of 4-nitropyridine from…

Q: Show the interconversions of acid derivatives using any branched six-carbon carboxylic acid. Include…

A: Organic chemistry.

Q: Please don't provide handwritten solution...

A: To synthesize hexane from the given reactants, which include 2-propanol and an alkyne, a series of…

Q: Provide a mechanism for the following reaction H₂SO4, H₂O HgSO4

A: This is a Mercury catalysed hydration reaction of an alkyne. The reaction occurs in strongly acidic…

Q: Complete the following reaction and provide a detailed, step-by-step mechanism for the process. HBr

A: It is an SN1 reaction. This reaction based on a more stable carbocation intermediate. First, alkene…

Q: How would you synthesize the following compounds from butanoic acid using reagents from the table?…

A: LiAlH4 is the reducing agent for the reduction of an aldehyde/ketone to an alcohol. Also, LiAlH4 is…

Q: Do not use carboxylation mechanism but show full mechanism for the question below

A: Step 1:• Firstly strong base i.e NaOEt abstract the acidic proton to forms enolate anion which…