-N* CH CI A

Q: A в

A: When A is treated with only C6H5Li (excess),  When A is treated with H2O,

Q: Draw the product formed when the α,β-unsaturated ketone A is treatedwith following reagent. H2…

A: Product of below reaction needs to be drawn:

Q: Draw the six products (including stereoisomers) formed when A is treated with NBS + hv.

A: The reagents that we can use is given as NBS which when used, through the free-radical mechanism…

Q: What reagent is best to complete the following reaction? ملا تملل OMe A) DIBAL B) 1. NaBH4 2. H+ C)…

A: Here we have to determine the best reagent among the following that can be used in the following…

Q: Draw the product obtained by heating each pair of ketones in a basic solution.

A: a.

Q: Draw the product formed from a Claisen reaction with the given starting materials using OEt, ELOH.…

A:

Q: Draw the complete arrow pushing mechanism for the base-catalyzed keto/en the following compound.…

A: The chemical equilibrium between ketonic and aldehydic form of same substance which get formed due…

Q: Draw the product(s) formed when A is treated with following reagent. LiAlH4, then H2O

A: Given reactant:

Q: Draw the products formed when A is treated with each reagent: (a) H2 + Pd-C; (b) mCPBA; (c) PCC; (d)…

A: Structure of Given molecule:

Q: What epoxide is formed when each alkene is treated with mCPBA?

A: Given compounds,

Q: by treating with NaNH2 follow a mechanism including curved arrows and intermediates for one. CH3 IV

A: Only terminal alkynes react with NaNH2 because it have acidic proton and NH2- is a strong base…

Q: NBS hv

A: Generally N-Bromosuccinimide is used in alkene for free radical substitution at allylic position…

Q: Draw the product(s) formed when A is treated with each reagent.a. NaBH4, CH3OH b. LiAlH4, then H2O…

A: The product(s) formed when A is treated with given reagent.

Q: Draw the product when attached compound is treated with either (CH3)2CuLi, followed by H2O, or…

A: The reagent, (CH3)2CuLi, is an organocuprate reagent, also called Gilman Reagent. Its general form…

Q: Draw the six products (including stereoisomers) formed when A is treated with NBS + hv.

A:

Q: What is major the product of this reaction? (H3C) 3C (A) (B) (C) (D) C6H5- HO C6H5 C6H5 H C6H5 C6H5…

A: The given reaction is an example of cross aldol condensation reaction .

Q: Identify A in the following reaction scheme, and draw a stepwise mechanism for the conversion of A…

A:

Q: Even though B contains three ester groups, a single Dieckmann product results when B is treated with…

A:

Q: Draw a stepwise mechanism for the following reaction.

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

Q: Draw the structure of compounds A–E in the following reaction scheme.

A: The given reaction is shown below. In order to obtain the structure of all the compounds, the…

Q: Draw the major product formed in attached reaction

A: Amine being a nucleophile can react with the alkyl halide. When an excess of CH3I is added to a…

Q: Draw the keto tautomer of attached enol.

A: Two molecules that have a similar molecular formula but differ in the way how their atoms are…

Q: What starting materials are needed to synthesize each attached compound by a Robinson annulation?

A: Robinson Annulation is an organic reaction that takes place between alpha-beta unsaturated carbonyl…

Q: Q.3 Give reason: a. Enols are considered as strong nucleophiles as compared to alkenes. b. Aldol…

A: Enolates are the anions which are derived from carbonyl compounds like aldehydes, ketones and…

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: What starting materials are needed to synthesize each compound using a Robinson annulation?

A: Part A

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

A: Amines act as bases as well as nucleophiles due to presence of lone pair on the nitrogen atom. On…

Q: How to draw product C? Please give detailed structure for the product C

A: here we are required to predict the product of the reaction

Q: Identify the acetal carbons in A, and draw the products formed by hydrolysisof A with aqueous acid.

A: An acetal carbon is a carbon atom which is attached to two ether group. The ether group are…

Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With…

A: SOCl2 reagent is used to convert acid into halide. This is one of the preferred pathway because the…

Q: Draw a mechanism for the following reaction: Br t-Buo

A: The mechanism for the following question is- The tert-butoxide was used to form alkene by the…

Q: Draw the products formed when A is treated with each reagent: (a) H2 + Pd-C; (b) mCPBA; (c) PCC; (d)…

A: a.

Q: Draw the product formed when A is treated with each series of reagents.a. [1] H2O; [2] NaH; [3]…

A: Compound A is a chloride derivative benzene diazonium salt and is prepared from aniline as follows:…

Q: How do I do this?

A:

Q: Draw a stepwise mechanism for the following reaction.

A: Ketones can be protected with the help of diols or thiols in acidic medium. In the given…

Q: Draw a stepwise mechanism for the following reaction. The four-membered ring in the starting…

A: The four membraned ring in the starting material and product is called as beta-lactum ring. DBN is a…

Q: Draw a stepwise mechanism for the following reaction.

A: In presence of H2SO4, alcohol undergoes dehydration reaction. For the given compound, the mechanism…

Q: Predict the major product when treated with H2/ Pd/c

A: Major product:

Q: Draw a stepwise mechanism showing how two alkylation products areformed in the following reaction.

A:

Q: Draw a stepwise mechanism for the following reaction.

A: The the gien reaction is called Haloform reaction.  presence of a methyl ketone is essential for the…

Q: Draw the product(s) formed when each alkene is treated with either [1] HBr alone; or [2] HBr in the…

A: Addition of HBr to alkene results in formation of alkyl bromide.  The product that is obtained when…

Q: pla Delow. Reage De us Map d0 than once or not at all. Draw the intermediate products B and C (both…

A: The first step is to start with acetylene as compound A, which react with strong base NaNH2. The…

Q: (a) Ignoring stereoisomers, what two allylic hydroperoxides are formed by the oxidation of hex-1-ene…

A: a). Oxidation reaction:In this oxidation reaction, hex-1-ene on treatment with O2 give two allylic…

Q: Draw the product formed when the α,β-unsaturated ketone A is treatedwith following reagent. [1]…

A:

Q: Draw a stepwise mechanism for the following reaction.

A: Given reaction,

Q: Draw a stepwise, detailed mechanism for the following intramolecular reaction that forms a cyclic…

A: The given reaction is  To find: The stepwise mechanism for the given intramolecular reaction

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.