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

Q: predict the product show the mechanism

A:

Q: Predict the product(s) and label the major product. Show the complete mechanism and name it if…

A: In the given question two reactions are given. In the first reaction, the ester reacts with alcohol…

Q: ? CH3CH2CH2C=CH + A) 2 Cl2

A:

Q: NBS.heat PRODUCT?? CHz NaCN PRODU CT 77 <

A: The final product of the reaction and mechanism has to be drawn.

Q: coph COOH Ccatalyst} sotvent

A: Wittig reaction is the reaction of an aldehyde or ketone with the ylide generated from a phosphonium…

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: predict product and show mechanism for the following mechanisms

A: Concept introduction: Addition of br2 molecule in Elkin is proceed to bromonium ion intermediate and…

Q: OH Br 3. Br pcc I) CH3 myBr 2)H30+ OH

A: PCC(Pyridiniumchlorochromate) is an oxidizing agent that oxidises secondary alcohol  into ketone.…

Q: R (or H) R (or H) HN 1. LIAIH (2) R 2. H20 R1 R. (or H) (or H) Imine (or H) (or H) Amine

A:

Q: REACTION #3 (1 elementary step): Name of Elementary Step:_ H Но + H. H. H REACTION #4 (1 elementary…

A: Following are the curved mechanism of the given organic reactions.

Q: Can you show the mechanism and explain the steps

A: Dehydration of alcohol in the presence of acid leads to the formation of an alkene.

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

A:

Q: rite product and mechanism

A: Since your question has multiple parts, we will answer the first part for you. If you want residual…

Q: „OCH, 1. LIOCH3,CH,OH H,CO" Product 2. Acid Work up

A: The given reaction conditions favors the "Dickmen condensation reaction" where the ester of…

Q: tBu!!!... CH3 CH3 KCN H₂O

A:

Q: C) NH2 CI Br heat

A: Given : To determine the above equation with mechanism.

Q: 1) O3; 2) HOOH 3) cat. H2SO4 CH3OH

A:

Q: Practice problems: draw the mechanism and products for the following Lewis acid/base reactions: F…

A: Lewis Acid: a species that accepts an electron pair (i.e., an electrophile) and will have vacant…

Q: HO CI OCCI3 NH2 CH2CI2, Et,N

A: The given reaction proceeds via nucleophilic addition elimination reaction mechanism at the carbonyl…

Q: What mechanism produced each product and why/how?

A: The mechanism of the given reaction is

Q: HO Д HC но 0 0 одн

A:

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: How is this incorrect and what is the correct mechanism?

A: Given : We have to tell what will be the correct mechanism.

Q: mechanism

A: 1- NaH, THF  2- Bn-Cl ( benzyl chloride ) = C6H5-CH2-Cl 3- LiAlH4

Q: What's the mechanism process to get this product

A: ylide formation

Q: We have seen that the alpha carbon atom of an enamine can function as a nucleophile in a Michael…

A: The question is based on organic reactions.     we need to identify the product formed and explain…

Q: OMS CH2CH2OH ?

A: Substitution reactions are of two types i.e. SN1 and SN2.In SN1 formation of carbocation takes place…

Q: Can you explain the mechanism? Can you provide a shortcut?

A:

Q: Hi/hegt HO.

A:

Q: ن PPh3 Product Starting materials

A: Designing an organic synthesis requires meticulously examining the target molecule, conceptualising…

Q: What product would you expect to obtain from Grignard reaction of an excess of phenylmagnesium…

A: The Grignard reagent gives a nucleophilic addition reaction with the dimethyl carbonate.

Q: (d) Cl₂ H2O CI """OH

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

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

A: The above reaction is known as oxymercuration demercuration.

Q: CH;CI b. CH3CECNa 1. H2C=0 CH;C=CNa 2. H30* С.

A:

Q: mawor product mC PBA NaBHy OCH; CH3 OH

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.