a. [1] [2] H,0 b. (] C6H5LI [2] H2O c. [1] Li н H. [2] H2O Li d. [1] CH2=O0 [2] H2O

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: Draw the product formed when each organometallic reagent is treated with H2O.

A:

Q: Draw a stepwise, detailed mechanism for the following reaction. но H+ CHO

A: At first the OH absorbs a proton turning itself into a good leaving group and then the double bond…

Q: хо Draw Enolate Anion + Draw carbonyl

A: Step 1:  Firstly ,  draw the structures for the original molecule. Step 2:  Structure of the Enolate…

Q: Match the correct reagents with each step A B

A: The starting reactant is an terminal alkyne to which a methyl, -CH3 group is added with the help of…

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Draw the stepwise mechanism for the following reaction. CH;CH2OH H2SO4

A: This is the reaction where the reaction proceeds via stable carbocation formation .

Q: Draw the product of the attached Claisen reaction.

A: The Clasien reaction is a condensation reaction in which carbon carbon bond formation takes place…

Q: How to draw any nucleophilic substitution product ?

A:

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

A: The given reaction is,

Q: Draw the most stable product formed in each of the reactions shown. Reaction (a) 2 مهر NaOEt, EtOH A…

A: In this question, we will draw the most stable product for this reaction inwhich two equivalent of…

Q: Draw the products of each reaction.

A: Given is organic reaction. The name of given reaction is hydrolysis reaction. The given starting…

Q: Draw a stepwise mechanism for the following reaction.

A: Since NaH is a strong base Hence it will remove the D from the reactant and form a -ve charge And…

Q: Drawing an SN1 Mechanism That Involves a Rearrangement Draw a stepwise mechanism for the following…

A: A stepwise mechanism for the following reaction has to be drawn.

Q: H₁ H KOH EtOH heat

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

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Draw the first intermediate and the final product.

A:

Reactive Intermediates

In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.

Hydride Shift

A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.

Vinylic Carbocation

A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.

Cycloheptatrienyl Cation

It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.

Stability of Vinyl Carbocation

Carbocations are positively charged carbon atoms.  It is also known as a carbonium ion.