d) The compound below exists in two tautomeric forms. Circde the most acidic proton in the keto form below and draw the enol tautomer of the compound. H.

Q: Explain: A) Please explain whether you would use heat or light in this transformation and why the…

A: Solution -

Q: Which carbon will be the best site for electrophilic aromatic substitution? A

A:

Q: HI (excess)

A: While writing the mechanism use electron pushing arrow from electron rich center to electron poor…

Q: The powerful electron-withdrawing property of a carbonyl group increases the acidity of a-protons…

A: The electronegativity of the carbonyl group is highest among other functional groups.

Q: Terminal alkyne is considered a more acidic compound because it has a lower s character. True or…

A: In this question, we will discuss about this Statement is true or false.  You can see details…

Q: Propose a plausible and logical synthetic pathway for the following

A:

Q: . Show how the enamine below can be synthesized. Then draw the resonance structure(s) for the…

A:

Q: Rank the following according to increasing reactivity with 1 as the least reactive, and 4 as the…

A: The reactivity order for nucleophilic acyl substitution is as follows:

Q: Terreic acid, shown below, is a naturally occurring antibiotic metabolite of the fungus Aspergillus…

A: Given molecule:

Q: From the given structures which is (a) an acid halide? (b) a secondary amide (c) an aldehyde…

A:

Q: Explain the following observation 1. Chlorine is orthor, Para deactivating group when attached to…

A: Answer:- This question is answered by using the simple concept of directive effects of the…

Q: he cyano group is often considered to be more stable than esters or even amides vhen reacting with a…

A: Introduction :  We have to tell why cyanide is a stable nucleophile.

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: A stepwise and detained mechanism for the given reaction can be shown below,

Q: k of the electrophile on the aromatic ring. neration of the stable aromatic system by loss of a p…

A: We need to draw the detailed mechanism for the chemical reaction.

Q: Which carbon will be the best site for electrophilic aromatic substitution? A C

A:

Q: A) Indicate the most acidic proton on each molecule. B) Rank in order from least to most which are…

A: Here we have to write the correct order of decreasing acidic strength of the following compounds and…

Q: Amides are weak nucleophiles but their conjugate bases are string nucleophiles. The amide drawn…

A: The deprotonation of amides can occur possible from two positions. The Bronsted-Lowry acid-base…

Q: 2. Draw a detailed mechanism for the following reaction.

A:

Q: Is a intramolecular Friedel Crafts acylation reaction. As you from the product, the acylation…

A: Applying concept of organic synthesis and reagent.

Q: O A successful Claisen condensation requires an ester starting material with at least one alpha…

A: Ketone alpha hydrogen is slightly acidic in nature. This is due to the stabilization of the…

Q: Which carbonyl contains the most acidic proton on its alpha carbon?

A: Acidity means release of hydrogen ions when dissolved in water. Organic reactions are those in which…

Q: Draw an enol tautomer of each of the following molecules. se &

A: Tautomers are structural isomerism. They are structurally different compound exist in dynamic…

Q: When naphthalene undergoes an irreversible electrophilic aromatic substitution, such as a…

A: Alpha position is more stable than beta position because

Q: Explain: A) Please explain whether you would use heat or light in this transformation and why the…

A:

Q: Question are attached

A: In question 1 structure b) contains more acidic H-atom .because after the removal of that H-atom the…

Q: Draw the product of the reaction and explain the reason OMe

A: Pericyclic reactions are proceeds by a cyclic shift of electrons by a single-step reaction…

Q: When compound A is treated with a strong base, a mixture of product B and C results. Which base…

A: Lithium base .  It is two types 1. Less hindered Lithium base 2. Highly hindered Lithium base.

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A: Electrophilic substitution is the substitution of H of an aromatic ring by an electrophile. The…

Q: an you select the answers in each bracket? The imine functionality is similar to [ carbonyl /…

A: Imine and enamine both are formed from reaction of aldehyde and ketone with amine

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: The above reaction is a diel's alder reaction in which a diene and and a dienophile undergo [2+4]…

Q: Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and…

A: Given reaction is acid base reaction,  According to Bronsted-Lowry theory , species which donates H+…

Q: The compound below exists in two tautomeric forms. Circle the most acidic proton in the keto form…

A: Keto and enol are form of tautomerism.

Q: Draw an enol tautomer of each of the following molecules.

A: Tautomers are structural isomers of chemical compound that readily interconvert. This result in the…

Q: Draw all enols of the following ketone.

A: Keto form is more stable than enol form

Q: And Allyl / Phenyl compound are most reactive towards SN2 because of resonance stabilization. then…

A: SN^2 reaction is a single step process. SN^1 reaction is a two step process. SN^1 reaction involves…

Q: What kinds of halides cannot be used to alkylate an amine? Why not? a.Tertiary halides form alkenes…

A: Correct Option :  d.  all of the above

Q: 1. reactivity towards nucleophilic acyl substitution CI HO, RANKING:

A: Nucleophile are those species which attacks on electron deficient species. In carboxylic acid and…

Q: Which compound in the following pair is more basic?

A: The resonance structures for pyrrole are given below -  While resonance structures of piridine are…

Q: H;C CH3 HN- -c-CH, A в a) Which of the above molecules (A or B) have a higher rate of reaction…

A: We have two compounds, we have to predict the rate of electrophilic aromatic substitution of the…

Q: base ? A B

A:

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A: If the compounds having similar structure, then the general trends of compounds reactivity in…

Q: retrosynthesis of the below targeted compound 'N'

A: Retrosynthesis is the process of breaking the target molecule imaginary in the mind in such a way so…

Q: Two methods convert an alkyl halide to a carboxylic acid having onemore carbon atom. Depending on…

A: Two methods convert an alkyl halide to a carboxylic acid having one more carbon atom. Depending on…

Q: Draw the organic product of the following nucleophilic substitution reaction. (Assume that only…

A: Given reaction,

Q: Chemistry Design a reasonable synthesis for the following transformation. E.

A:

Q: Draw the hyperconjugation interaction that lessens the electrophilicity of the carbonyl on the…

A: The answer is as follows:

Q: Rank the compounds in attached group in order of increasing basicity.

A: The higher the pKa value, the stronger will be the base or the lower the pKb value, the stronger…

Q: Propose a forward synthesis for one of the two sequences below using whatever reagents necessary. Do…

A:

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.