Propose a predict the major product in each of the following reactions

Q: Predict the MAJOR product by proposing a plausible mechanism. Indicate stereochemistry when…

A: NaH is metal hydride  In presennce of OH group which is higly acidic react with OH and acid-base…

Q: For the following structure, (a) propose the starting materials necess it through an aldol reaction.…

A: When aldehyde and ketone having α-hydrogen are treated with dilute alkali , forms β-hydroxy…

Q: Below is one of four steps in an electrophilic aromatic substitution reaction. Braw the curved arre…

A:

Q: OMe ? Me OMe ОН

A:

Q: Synthesize the following compound via Claisen condensation and any other necessary reagent.

A:

Q: Provide/ Draw the major product/s of the following reactions

A:

Q: Predict the major product of the following reaction ICI

A:

Q: H.

A: Based on the following transformation, provide or propose an efficient synthesis

Q: Propose a plausible synthesis for each of the following transformations:

A:

Q: a) (b) ON c)

A: The given compounds are synthesized from alkyl halide and aldehyde or ketone has to be given.

Q: Predict the MAJOR product for the following reaction:

A:

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

A:

Q: Predict the major product for the following reaction:

A: •When phenol react with acid anhydride give phenyl ester. •Here nucleophilic substitution occur.

Q: Give the major elimination product derived from each of the following elimination reactions. Pay…

A:

Q: Provide

A: According to the question, we need to determine the major product of the monobromination reaction.

Q: Provide the major product and indicate which mechanism

A:

Q: Propose a plausible synthesis for each of the following transformations:

A: For the above conversion, the steps involved are abstraction of proton from alkyne, nucleophilic…

Q: エZ

A: Here we have to synthesize the given compound by suitable starting materials.

Q: 8. Propose an efficient synthesis of for each of the following transformation: a) b) EtO OEt

A: Many reagents are used for the conversion of one compound to another. A chemical reaction takes…

Q: Predict the major product for each of the following reactions:

A:

Q: La AICI, A B D

A:

Q: please help with this question. thank you. Propose an efficient synthesis of for each of the…

A: 1. Alkenes upon ozonolysis to give carbonyl compounds , alpha hydrogen containing carbonyl…

Q: Predict the MAJOR product by proposing a plausible step by step mechanism. Indicate stereochemistry…

A: Ring opening  of epoxides  in acidic  medium  through  SN1 Type mechanism  attack preferred.

Q: Predict the major product for the following reactions

A: Here is your answer

Q: a) Provide the organic starting materials necessary to synthesize the following compound via an…

A: I solved only one question. Remaining repost

Q: V. Propose a plausible synthesis for each of the following transformations: CI CI 1.

A:

Q: Based on the following transformation, provide or propose an efficient synthesis

A:

Q: Rank the following carbonyls from the least to the most reactive towards a nucleophilic, provide a…

A: Aldehyde and ketone both combindly called carbonyl compounds In carbonyl group , carbonyl carbon…

Q: он

A:

Q: Predict the major product for the following reaction.

A:

Q: Use the EAA or DEM synthesis and show how you would prepare each of

A:

Q: Predict the major product for the following reactions. Be sure to include stereochemistry when…

A:

Q: Provide all reagents to accomplish the following synthesis:

A: NBS is N-bromosuccinimide is used for allylic substitution. Thus Br group is substituted at the…

Q: Predict the major product in the following reactions:

A:

Q: Propose an efficient synthesis for each of the following transformations: .CI

A:

Q: Predict the major product in following reaction sequence (sh

A:

Q: Propose a mechanism for each of the following reactions

A: The given reaction:

Q: Predict the Major product for the following reaction.

A:

Q: Provide the major substitution product for each of the following reactions:

A: We have to predict the product of the given reaction.

Q: 13. Show a curved arrow mechanismand predict the major product for the following reactions.

A:

Q: Propose a two reaction sequence to convert each of the following substrates into the indicated…

A:

Q: Propose a plausible synthesis for each of the following transformations a.

A: Synthesis is given below.

Q: HBr peroxides

A:

Q: но.

A: A detail solution is given below -

Q: conc. HNO3 conc. H2SO4 `OCH3 Fuming H2SO4

A: Given,

Q: IV. Propose an efficient synthesis for each of the following transformations: -A он "OMe

A: Note: According to our guidelines we are supposed to answer only first three subpart.  Kindly repost…

Q: CH3CO3H CH3COCI pyridine

A:

Q: HC HC

A:

Q: Predict the major product for each reaction:

A: At first alkene being nucleophilic undergo protonation to give most stable tertiary carbocation.…

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.