HNO3 `NH `NH H2SO4 NO2 Acetanilide para-Nitroacetanilide

Q: Draw all constitutional isomers formed in attached elimination reaction. Label the mechanism as E2…

A: The base and the type of alkyl halide in a given reaction determine the mechanism. In the given…

Q: `NH HNO3 `NH H2SO4 NO2 Acetanilide para-Nitroacetanilide

A: We have to draw the curly arrow mechanism for this reaction showing step by step and also draw two…

Q: B. In each of the following pairs, circle the species that is more reactive toward nucleophilic…

A: We know that greater electrophilicity of  the carbonyl, then faster will be the nucleophilic attack

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A: Proton abstraction from the acid HCl. Nucleophilic attack on to the carbonyl carbon by the lone…

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Q: (a) p-Nitrobenzaldehyde is reactive toward nucleophilic additions than p- more methoxybenzaldehyde.…

A: a)

Q: Which of the following compounds will dissolve in aqueous NaOH after undergoing reaction with…

A: We have to predict the compound that can be dissolved in NaOH.

Q: F

A:

Q: Hydroxy aldehydes A and B readily cyclize to form hemiacetals. Draw the stereoisomers formed in this…

A: The formation of a cyclic hemiacetal is an acid catalyzed reaction. The cyclic hemiacetals formed by…

Q: Why is it important to proceed with the acetanilide formation before the nitration? The nitration is…

A:

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

A: Given molecule:

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A: The acyl substitution reactivity order is given as :-  Amide < Ester < Acid anhydride <…

Q: DHG (OACameay

A: The above-given reaction is an example of Oxymercuration demarcation reaction:

Q: 3. What, in general, is the order of decreasing reactivity of these carbonyl compounds towards…

A: In an organic reaction, a nucleophile which is electron rich attacks an electrophile which is…

Q: Match the reagent on the left in the list below with the product formed on the right when the…

A: Reaction 1: cyclohexanone reaction with Hydroxyl amine gives oxime. Reaction 2: Cyclohexanone…

Q: This question has multiple parts. Work all the parts to get the most points. The Stork reaction is a…

A:

Q: Which reagents could be combined to make the following in a reasonable number of steps and order?…

A: Reaction step - In these reaction sequence first we hydrolyse ester into acetic acid and ethyl…

Q: I cyclohexanone II cyclohexanol III methylcyclohexanol. (b) Arrange the above compounds in the…

A:

Q: What is predominant reaction type between 2- bromopentane with sodium ethoxide? O SN1 SN2 O E2 E1

A: 2-bromo pentane with sodium ethoxide  Reaction predominant type is ...

Q: NH2 NHCOCH3 H/H2O (Hydrolysis) NO2 ÑO2 p-Nitroacetanilide (major) p-Nitroaniline

A:

Q: B) Rank the following compounds toward increasing acidity, , why? 2) 1,3-benzoqounoin…

A: The acidic order depends on two factor  1) how fast the given compound release H+ ions  2) the…

Q: Draw all constitutional isomers formed in attached elimination reaction.Label the mechanism as E2 or…

A: The given reaction is,

Q: `NH HNO3 `NH H2SO4 NO2 Acetanilide para-Nitroacetanilide

A: We have to draw two alternative isomers of nitroacetanilide and suggest two reasons why, during this…

Q: Explain why compound A does not undergo an E2 elimination with strong base.

A: For the structure to be more stable it has to have the bulky phenyl group in the equtorial position.…

Q: A primary arylamine treated with nitrous acid is converted to a arenediazonium salt whose leaving…

A: We have to understand what is the leaving group of aryldiazonium salt derived from primary aryl…

Q: When a carbonyl compound is attacked by a nucleophile resulting in the formation of a new…

A: In the carbonyl compound nucleophilic addition reaction occurs.

Q: Rank the compounds in each group in order of increasing reactivity in nucleophilic acyl…

A: Weak bases are good leaving groups. Reactivity of carboxylic derivatives depends on the leaving…

Q: Intramolecular reactions are also observed in Friedel–Crafts alkylation. Draw the intramolecular…

A: (a)

Q: Example #1: Predict the substitution pattern when this compound undergoes a sulfonation reaction. |…

A: • Sulfonation reaction Electrophile is SO3⊕H.• Friedel-Crafts alkylation Electrophile is → R-⊕

Q: Consider the following groups of compounds. In each series circke the weaker (poorer) nucleophile.…

A: The nucleophilicity of a substrate depends upon many factors such as basicity, nature of…

Q: The compound below can undergo E2 reaction mechanism upon addition of sodium chloride. F Select one:…

A: Elimination reaction of alkyl halide: Alkyl halide gives an elimination reaction by reacting with a…

Q: Acetal product formation is difficult since hemiacetals are stable while acetals are not. True False

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Q: Rank the compounds in each group in order of increasing reactivity in nucleophilic acyl…

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Q: Explain why the C=C of an enol is more nucleophilic than the C=C of an alkene, despite the fact that…

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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: reactivities of the following compounds according to the SN1 reaction. please explain why a) Methyl…

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Q: What is/are the proper descriptor(s) of the product of the following reaction? HN and trace acid O…

A: Ro answer this question , we would first write the product of the reaction. Then we can check the…

Q: NO2

A:

Q: Rank the derivatives of phenol in order of increasing acidity (Please explain) 

A: The compounds given are,

Q: 7. Propose an efficient synthesis of for each of the following transformation: a) b)

A:

Q: 4-Methylpyridine reacts with benzaldehyde (C6H5CHO) in the presence of base to form A. (a) Draw a…

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Q: F3C² CF₂ reactive acyl Most -nucleophilic اعم least substitution H3C reactive CH3 3 to word

A: Dear student since you have asked multiple questions but according to guidelines we will solve 1st…

Q: The follow ing compound can be synthesized by a mixed Claisen condensation. Identify the two…

A: Claisen condensation reaction is a reaction between two esters in presence of strong base to form…

Q: Explain why electrophilic aromatic substitution in Pyrrole takes place at C-2 positions whereas, in…

A: Note: according to our guidelines we are supposed to answer only one question

Q: Draw a stepwise mechanism for the following reaction: H,SO, Part 1: A. HSO, B. H,SO, C. H,0 view…

A: The reaction taking place is given as,

Q: Arrange the following benzyl anions in the increasing order of stability. Substantiate your stand.…

A:

Q: structure of N-ethyl-N-methycyclobutanamide i

A: The structure of a molecule gives the arrangement of atoms in space.

Q: Alkyl halides 1-chlorobutane 2-chlorobutane Allyl chloride 2-chloro-2-methylpropane…

A: This question basically requires the basic concept of understanding the stability of carbocation.…

Q: (c) What is the solvent effect on the SN1 and SN2 reactions?', (d) Which reactant in each of the…

A: In SN1 carbocation intermediate is formed.. And in SN2 transition state is formed..

Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.