NaOEt, ELOH Product EtO

Q: Perform the following retrosynthesis. (Provide the reactants and reagents required to convert the…

A: The hydroxylation of species alkene will occur in the sight of molecule osmium tetroxide OsO4 along…

Q: (d). 1. MgBr 1. O3 (2 equivalents) 2. Me,s 2. H20

A: Organic compounds in which two carbon atoms of a hydrocarbon chain are bonded to each other by a…

Q: mechanisms of this reaction

A:

Q: CH,OH /H° ОН ANISM

A: - given compound is the carboxylic acid  Which reacts with the alcohol in presence of acidic…

Q: H. NH2

A: The reaction taking place is given as,

Q: OH ONLY CI

A: See synthesis below.

Q: OH HO Br HO

A: The question is based on the concept of chemical conversions. we have been given reactant and…

Q: NaH Br

A:

Q: What is the mechanism for the following reaction?

A: Given reaction,

Q: OTs NaOEt ELOH

A:

Q: b. dry acetone . + OH

A: The product formed is 1-methylcyclohex-1-ene.  Mechanism: The hydroxyl ions abstract the alpha…

Q: Me Me Ме Me Ме H20 Br Br HO. + Но H Et Et RDS Et H Et Et transition state carbocation intermediate 우

A:

Q: Give the major product of the following reaction. MeO H2

A: Given,

Q: Br NaOCH3

A:

Q: S. Classify the following reagents as either nucleophiles or electrophiles: Znt, CH,NH2, HS, OH, ,…

A: Since we answer only one question. So, we'll answer the first question. Please resubmit the question…

Q: NgOH, EtoH. HO (+H20 + NaCI)

A:

Q: Br NaOEt ELOH

A: Elimination resulEts in formation of Alkene.  Elimination can proceed in presence of Acid Or Base.…

Q: Notice in Problem 25.63 that the hydroperoxide forms at the C atom that is α to the O atom and not…

A: A free radical chain reaction involves free radicals in a cyclic sequence of steps, called…

Q: OMe cm Clz mCP BA MeO `OH

A: Given reaction is example of Baeyer-Villiger oxidation. The Baeyer–Villiger oxidation is an organic…

Q: MeH Ме ОН N. H. Fill in the necessary reagents to complete the given reaction.

A: Reaction 1 : At ring junction methyl and hydrogen are trans. In the product Me and H are opposite…

Q: What is the product and mechanism? b. + OH dry acetone .

A: 1°>2°>3° Then Acidity order is also 1°>2°>3°

Q: ? OCH3

A: Carboxylic acid reacts with the two molecules of the Grignard reagent to form the tertiary alcohol.…

Q: Propose a mechanism for attached reaction:

A:

Q: HCI cold

A:

Q: 3. Show the reasonable curved mechanism for the reaction and make sure lone pairs Y Ocuk + Conc HBr…

A: (a) Lone pair of oxygen is acting as a HOMO and antibonding orbital of H-Br bond is acting as a…

Q: HO OH Br HO

A: synthesis of grignard reagent from alkyl halide attack of grignard reagent (as nucleophile) to…

Q: Question attached

A: In an organic reaction, a nucleophile attacks an electrophile.

Q: TSOH MeOH

A: Product for the given reaction is,

Q: CH3OCH₂CI BuLi OH H* Product Product H* Product

A:

Q: show me and explain the mechanism for this reaction please

A: In the above reaction, since the alcohol is 2 degree, hence the reaction is happening  The above…

Q: OTs NaOEt ELOH

A: The OTs group gets eliminated in presence of strong base like NaOEt and EtOH and alkene is formed as…

Q: CHO CHO MeO

A: Diels-Alder reaction: The Diels–Alder reaction is a pericyclic reaction (cycloaddition) between a…

Q: Provide the mechanism and the product for the following reaction: Br* MeOH

A: A species having a positive charge is known as the electrophile whereas the species having electron…

Q: Catelyst Rucly CPPh37, me

A:

Q: Can someone please show me a step by step mechanism of this reaction?

A: The given reaction is

Q: + ČH3 azulene

A: Cyclopentadienyl anion acts as a nucleophile while N-methylpyridine as an electrophile. Reaction…

Q: NABH., MeOH Product он он OH OH но, но. он

A: Sodium boron hydride is a mild reducing agent

Q: Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible…

A: The complete reaction is given below.

Q: R `OOH

A:

Q: ? a. HO. b. NH, N. d.

A:

Q: НО H2SO4 heat

A:

Q: .ce AICly

A: This is the friedelcraft reaction .

Q: *NH H*

A: Reactants are secondary amine and ketone, medium of reaction is acidic medium.

Q: N H .N. NaNH2 CI CI

A:

Q: ROOR

A: Here the reagent is an alkene and it is being treated with ROOR.

Q: Acetals react with: O PhLi, phenyllithium NaOCH3, sodium methoxide EtMgBr, ethyl Grignard О НЗО+ O…

A:

Q: 6- Complete the mechanism of the following reaction? HO TSOH, OH + H20

A: The given reaction is an acid-catalyzed cyclic ketal formation. The resulted ketal is a spirocyclic…

Q: Select the major organic product of this reaction. PCC HO, product

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.