The final product, E, in the following reaction sequence is, PBr3 Mg A CH;0 B. H;O - D PCC OH ether CH;Cl,

Q: :0: :0:- CH3 - CH2-C- CH3 OH CH3-CH=C-CH3

A: Ans

Q: MgBr Acid 2

A: Organic reaction.

Q: ce CH3-C=CH 2 Hce CH3-C-CH3 ce

A: In the first step the terminal carbon atom of the alkyne will get protonated by one HCl molecule.…

Q: The major product formed in the reaction below is:

A:

Q: H20 H2SO4

A:

Q: The major organic product in the reaction sequence below is:

A:

Q: The major product formed in the reaction below is:

A: The given reagents are - 1. BH3, THF = this reagent will attack the double bond. 2. H2O2, NaOH, H2O…

Q: CI 2HCI CH3-CECH CH3-C-CH3 CI

A:

Q: The major organic product in the reaction sequence below is:

A: The reaction of alcohol with NaH in the presence of alkyl halide results in the formation of ether.…

Q: The major product formed in the reaction below is:

A: When any aryl bromide (or alkyl bromide) undergoes a reaction with ethanolic KOH, the beta-hydrogen…

Q: The major product formed in the reaction below is:

A: In this given sequence of reaction, first, the sodium salt of acetylene would react with an alkyl…

Q: The major organic product in the reaction sequence below is:

A:

Q: NO2 HBF4 Br, FeBra H2, Ni NANO2, H0*

A: We have to predict the major product from the given reagents.

Q: the major product in the reaction sequence below is:

A: As given, the reaction proceeds through the usage of peroxides thus the reaction will take place…

Q: Complete the following reaction below:

A: We have to Complete the given reaction

Q: The major product formed in the reaction below is:

A: The given reagents used are - 1. Hg(OAc)2 = It is the reagent for oxymercuration-demercuration…

Q: O mCPBA ?

A:

Q: но ногом 0 Н. ен Н. за у (osnx7) Н -он

A:

Q: Step 1: Step 2: No OCT Sodium hypochlorite наё + со ясно cyclohexandl ما H30+ acid Co acetic acid +…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Ph 1 2 3 4 Br NaCN 1. LIAIH4 2. HO Ph 1 Ph رسید NO2 3 NH Ph Ph 2 4 *NH2 NH2

A:

Q: 0 K N₂ A H₂O Asco COH

A:

Q: Predict the product given the following reaction mechanism below

A:

Q: 2 equualents of CH3CH2MGBV BrZ

A:

Q: NaCN NH3 NaN3 NH reagents/solvents of your choosing ?

A: This question is from basic reaction mechanism.

Q: CH3 a) CH;C=CH, + HCl → CH3 b) CH;C=CH2 + HBr CH3 H+ c) CH;C=CH2 + H2O CH3 H+ d) CH;C=CH, + CH;OH

A: Applying concept of organic synthesis.

Q: The major product formed in the reaction below is:

A: The reagent H2(g), Lindlar catalyst will attack the triple bond and would convert it into the cis…

Q: Which of the following reactions willactually yield the indicated product?

A: The given following reaction is actually yield the indicated product can be identified

Q: What is the major product is expected in the following reaction

A: Given : We have to make the major product for the following reaction.

Q: the major product formed in the reaction below is:

A: Epoxidation : Per-acids are very good epoxidising agent.  e.g. CH3COOOH is called peroxy-acetic…

Q: the major product formed in the reaction below is:

A: Sodium ethoxide would react with the cyclohexyl bromide and would replace the bromide ion. And the…

Q: H2 1. Вн/THF A В Lindlar 2. Он, Н-О2, Н,0

A:

Q: What is the synthesis and mechanism for the following?

A: Hofmann's Rule: It is elimination reaction in which the formation of alkene from rather most…

Q: The mechanism by which the following product is formed is:

A: In the above reaction, the alcohol reacts with the acid to produce water and alkene.

Q: Provide the major organic product of the reaction below. HBr

A:

Q: 인 + CH3OH

A: Elimination reaction-: The chemical reaction in which a simple molecule like H2O,HX or X2 etc are…

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.