find the product (name too) from this reaction and draw the mechanism as well showing arrows

Q: Br

A: The important information to note for the given problem is:   It specifies the need of Wittig…

Q: HNO3 1 СНО -OH ОН NH,NHPH 2 -OH H- -OH ОН NABH4 CH,OH エエエ

A:

Q: ? CH3CH2CH2C=CH + A) 2 Cl2

A:

Q: Draw a curved arrow mechanism for the reaction. Add steps as necessary and be sure to add lone pairs…

A: Elimination reactions involve the removal of atoms or groups to form the alkenes. The elimination…

Q: L H Z NN H I I P Br E c > C [

A: When carboxylic acid reacts with ammonia the final product of this reaction is amide.

Q: Solvolysts ~predictall possible products for this svotverysus Teaction. Show the mechanism, and…

A: The given reaction condition is E1/SN1. In this removal of bromide ion in the rate determining step…

Q: desired product actual product 1. LDA, -78 °C 2. CH3BR Explanation: HO 3-Br/ HO. CH3

A: In the given reaction, LDA (Lithium Diisopropylamide) acts as a strong base and abstracts the most…

Q: 8-3. Michael addition * BuOk ㅋ A uiche el puduct

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Draw the organic product(s) you would expect from the following reaction. CH3 H3C **** + Br₂ (1…

A: The bromination of a conjugated alkene involves the addition of bromine (Br2) to the double bond of…

Q: Please draw the products and please answer questions A through E

A: The solutions are

Q: NBS, ROOR

A: The reaction taking place is given as,

Q: Draw Diene Drawing a

A: The reaction between a conjugated diene and a dienophile forms an unsaturated six-membered ring.…

Q: mutistriatin Hg C -CH3 3C H+ H2 O

A:

Q: Problem 20 of 50 H₂C H Select to Add Arrows H Select to Add Arrows Submit

A: Given is carbanion molecule.Carbanion is species in which carbon carries negative charge.Curved…

Q: LIAIH4 H20

A: Lithium aluminium hydride is a very good reducing agent used in the reduction of aldehydes, ketones,…

Q: tBu!!!... CH3 CH3 KCN H₂O

A:

Q: & + CH30Ⓒ H3CO +

A: The reaction involves two steps.  1. Nucleophilic attack of OCH3- to the less hindered carbon of…

Q: . Predict Drodvets for reacticn 2.Draw Ane Products) are Majar chanism and indicate which H3

A: Interpretation- To predict the product and propose mechanism for formation of major product.

Q: (vi) 2 -CH2-Li 2. 1. Cul Br

A: This question is base on Gilman reagent . Gilman reagent is a nucleophilic.  Use for formation of…

Q: Which reagents would best accomplish this transformation? %3D .C. HO, CH3 CH3 CH3 (A) K,Cr,O, +…

A: The reaction given is,

Q: f) of 1- 2- H* Br 3- H*, H₂O 1-03, CH₂Cl2, -78 °C 2- CH3SCH3 C8H1402

A: Given,The reaction:

Q: 1. HBr 2. МеОН, н* O. 3. MеР(ОE()2 4. Нао"

A: The product formed in the given reaction is, The first step is the hydrolysis of given substrate…

Q: Predict Droduets for reactich Draw Ahe Mechanism and indiCate whic ProducAfs) dre NMa

A: The product of the reaction can be predicted as

Q: 1) LIAIH4, Et,0 H. 2) H30* 3) NaH (excess) 4) CH31 (excess)

A: Step 1 - All carbonyl functional group reducted by LiAlH4 with acidic work up. Step2- Deprotonation…

Q: Show a mechanism with curved arrows for the reaction.

A: The given reaction is,

Q: а) b) C) 6 2 OH CHO ОН OH HNO₂ NaOH HNO, К.С 20, H.SO. НО CH₂OH ОН OH OH COOH

A:

Q: Draw the MAJOR product(s) for each of the following reactions. Br ELOH NBS hv NaBr OTs Br2 Br hv…

A: Draw Major product

Q: Question: How to synthesize the following four compounds from ethyl benzene? 1. 2. 3. 4. Br OH o OH

A: In this question, we will synthesized the following compounds from the starting material…

Q: NO₂ CI Name, Aheat H30+

A: Given:   This Reaction follows Addition - Elimination Mechanism.

Q: predict final product Show mochanism of tautomerizatio Nine 1.9-BBN Z. NGOH , HZD z

A:

Q: ОН о 1. H2NNH2, H+ 2. КОН, Д он

A: The Wolff-Kishner reduction is a reaction used to convert carbonyl functionalities into methylene…

Q: مله HO

A:

Q: H. CI

A: The given reaction is a simple SN1 reaction of 2 methyl propane with HCl to form 2 chloropropane.…

Q: Cl Mg ether CH₂CH₂OH

A:

Q: 1) Hg(OAc)2, H20 2) NaOH, NABH4

A: The above reaction is known as oxymercuration demercuration.

Q: Synthesize the (target) molecules on the right from the starting molecules the left. Give reagents…

A: The question is based on the concept of organic synthesis. We need to synthesize the product using…

Q: 4- Propose a synthetic pathway for each of the following compound Show all steps. Starting from…

A: The given compound has an alkyl group substituted at the para position. The first step in the…

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.