Expalin estrification mechanism from which point oxygen is elimate.

Q: Draw the products of attached reaction.

A:

Q: acture of the major organic pr«

A:

Q: Draw the arrow pushing mechanism for the following reaction

A: The reaction of an alkene with HBr is complete in 2 steps – Formation of carbocation Nucleophilic…

Q: provide prod. will it be disrotatory or conrotatory process?

A: Organic compounds can be defined as the compounds that are made up of carbon and hydrogen atoms in a…

Q: The heat of reaction (evolution or absorption) is associated with

A: Heat of a reaction is the amount of heat evolved or absorbed during a chemical reaction taking place…

Q: Choose the best answer. Which of the following has similar preferred site ( carbon #) for…

A: The solution of the question is given below:

Q: Synthethic

A: 1- EtOH, H+ ( Formation of ester bond ) 2- H2, Pd(C) [ removing of protecting group )  3- K2Cr2O7,…

Q: do the acetal forming mechanism

A: Given that, we have to show the mechanism for the formation of acetal.

Q: Is it possible to synthesize from these two when cutting in this way? Also, please explain the…

A: The provided retrosynthesis will not work for the synthesis of given target molecule. This…

Q: Indicate the true clectrophile that is used to odd to Hhe aromatic ring in Acylation reachion

A: In this question, we will indicate true Electronphile for aromatic acylation Reaction.  How we can…

Q: indozolin(i) from CH2COOC2H5 N OH

A: Indozoline is prearped from Chchibabin reaction

Q: What alkene yields attached set of oxidative cleavage products ?

A: Concept introduction: Ozonolysis: It is the process in which ozone is added to alkene and form…

Q: which of these has tautorimzation occur during the mech of the final product

A: Tautomers are isomers of a compound which differ only in the position of the protons and electrons.…

Q: tow is benzophenone suited for nueleophilie aromaic abstitution Which positions and the be…

A:

Q: Provide a Curved Arrow Mechanism for the following reaction. .CI HO- HCI

A: The above reaction is an example of a substitution reaction where the reaction goes through a…

Q: Dissociative interchange mechanism

A: Dissociative substitution describes a pathway by which compounds interchange ligands. The term is…

Q: Ph Ph ZI

A: Ans

Q: your performed a Ad extraction Iquid-liquid to isolate isopentyl acetate every the isopentyl acetate…

A:

Q: synthesized calcitriol in *

A: Here fill in the blank question is  given.

Q: Draw the arrow pushing mechanism of the following reaction

A: Given substrate is 3°alkylhalide hence in presence of polar solvent and heating conditions favours…

Q: b) Visualise following instructed) (i) the retrosynthesis for the target compounds (as along with…

A:

Q: Synthesis of benzoin

A: Coenzyme synthesis of benzoin

Q: ) Complete the following Oxymercuration-demercuration reaction. (Pay attention to the…

A: In oxymercuration and demercuration (OMDM) an alkene is treated with Hg(OAc)2 and the product is…

Q: HCI (b)

A:

Q: In micxed aldol condensation of acetone with excess benzaldehyde in the presence of NaOH: it is…

A: We have to draw the result from a single condensation reaction when micxed aldol condensation of…

Q: For the following reaction step, indicate which pattern of arow pushing it represents. O proton…

A: From the given reaction step : indicates which pattern of arrow pushing it represents ?

Q: (c) Provide two different yet valid for the following retrosyntheses compound (with synthesis). off

A: Synthetic planning starts with the final product ( target molecule) , which is fixed and…

Q: Give tha synthesis of oxamniquine with mechanism

A: The oxamniquine is a drug

Q: Can you explain the mechanism? And can you give any shortcut to use on tbe test

A: Consider the mechanism divided into steps as follows:

Q: DA. One product is formed, and it is achiral.

A: A carbon center which is sp3 hybridized and is bonded to four different atoms is called chiral. NaH…

Q: Propose a mechanism for the α,β-elimination reaction.

A: A mechanism for the α,β-elimination reaction has to be given

Q: Eom form a synthetic pathway 6or tanget molecule Stauting mateuials must a maximum of 6 Carbons and…

A:

Q: Synthesize attached product from the given starting materials using an organocuprate coupling…

A: Product from the given starting materials using an organocuprate coupling reaction has to be given.

Q: Propose Mechanism to get the follwing synthetic target

A: An organic reaction mechanism is a complete step by step account of how a reaction of organic…

Q: Draw the synthetic pathway including reagants + products

A: The question is based on the concept of organic reactions.   we have to convert given reactant into…

Q: What is the stepwise mechanism

A: The reactions involving organic compounds are called organic reactions.  Organic reactions are of…

Q: what is the plausible synthesis?

A:

Q: complete the following synthesis produces using a proper reagent and products

A: Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional…

Q: Draw a stepwise mechanism for the attached reaction. (Hint: Conjugateaddition can occur with…

A: Nucleophilic Conjugate addition reaction: The reaction will take place when In  α-β unsaturated…

Q: For each of the following compounds, identify them as being a nucleophile (Nu) electrophile (E). or

A: Electrophile is a chemical species which accept electron pair and which is deficient in nature where…

Q: draw a curved arrow mechanism of the following reaction, draw the two intermediate structures and…

A: Electrophilic aromatic sbstitution reaction (EASR) :  First Electrophile is added to double bond…

Q: (a) What is umpolung? for Write the mechanism synthesis from the of 1-acetyl-2-cyclohexen-1-ol…

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Q: najor product of the following reaction

A:

Q: Devise a synthesis of attached compound from the indicated starting material.

A: Benzene is an aromatic compound which contain electron density and is attacked by the electrophiles.…

Q: CI- from Br Synthesize

A: ->Aromatic compounds give electrophilic aromatic substitution reaction. ->In Friedel craft…

Q: S) Prndea nablemechanism for tre reaction Hices?

A: Cleavage of ether in presence of HI.

Q: for this reaction scheme suggest a reagent that could be used to accomplish the first step and draw…

A: Alcohols on reaction with sodium metal forms sodium alkoxide . R-OH + Na ------> R-O-Na+ Sodium…

Q: Provide a Curved Arrow Mechanism for the following reaction. .CI HO. HCI

A:

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.