Complete the reaction scheme

Q: 'N- CI

A: We have to carry out given synthesis. The required synthesis are shown below

Q: Draw the arrow pushing mechanism for the following reaction

A: The reaction of an alkene with HBr is complete in 2 steps – Formation of carbocation Nucleophilic…

Q: give the major products of each reaction

A: We have given three organic reactions.  Major product : the major product of reaction is the product…

Q: Give the products of each reaction.

A: Here we are required to find the product of the reaction

Q: Identify (label) the electrophile and the nucleophile in the reaction and add curved arrows to the…

A: The specie which is electron deficient is known as electrophile and the specie which is electron…

Q: do the acetal forming mechanism

A: Given that, we have to show the mechanism for the formation of acetal.

Q: Draw the organic product of the reaction.

A: This is the esterification reaction in which is taken from carboxylic acid and hydrogen is taken…

Q: How Nucleophilic substitution occurs ?

A: The transfer of electrons from the nucleophile to the substrate takes place in a nucleophilic…

Q: at changes in color take place when KMnO4 reacts with an alkene

A: To tell the change in color when KMnO4 reacts with an alkene.

Q: Why alkyl groups considered as an ortho- , para-directing?

A: To find: Why alkyl groups are considered as an ortho-, para-direction

Q: Reaction Method: Reaction Mechanism Sublimation, Elimination, Reaction with Metal, Ester Formation,…

A: Type of reactions: 1). Physical transformation reactions:  Sublimation reaction : it's a phase…

Q: Copy the given reactions and supply curved arrows to account for the formation of the products.

A:

Q: Select the appropriate sequence of reactions to accomplish the following synthesis.

A: The starting material ethyl methyl ketone contains active methylene group and so undergoes…

Q: Draw curved arrows to show the movement of electrons that illustrates the mechanism of the reaction.

A: Nucleophile prefer to attack to that site which has deficiency of electrons.  Due to high…

Q: Reduction

A: The above Reaction is the Reduction reaction of the Ketone . We can carry out the Reduction reaction…

Q: What is the appropriate electrophile nucleophile and solvent to achieve this final product

A:

Q: Draw the arrow pushing mechanism of the following reaction

A: Given substrate is 3°alkylhalide hence in presence of polar solvent and heating conditions favours…

Q: what is the major product of the reaction

A: We have to predict the major product of given reaction.

Q: Draw curved arrows to indicate the movement of electrons in the following reaction.

A:

Q: CAN HO

A:

Q: Draw the arrow-pushing mechanism for this reaction.

A: In this , an equilibrium is shown where an alcohol and enol form are in equilibrium with each other.…

Q: What is the final product of the following reaction:

A:

Q: Give the product to complete the reaction. Indicate NR if there is nor reaction.

A:

Q: How is this compound synthesized with its chemical reaction mechanism

A: Let us discuss the step by step process of aspartame synthesis.

Q: I need the reaction mechanism of this synthesis

A: Welcome to bartleby !

Q: Which can ot be used in the second step of the reaction sequence

A: Azide ion is a strong nucleophile (far better than amines) and will readily participate in…

Q: Which will react slower in polar protic solvents

A: Polar protic solvent is polar solvent.

Q: AICI

A:

Q: Given the data, find the specific heat of part A;     Heat of Reaction 1 (ΔH1) of part B;…

A: Provided data:

Q: What type of carbocation is shown? (+)

A:

Q: This reaction can be completed with which reagents?

A:

Q: Draw the major product of this reaction. Ignore inorganic byproducts and the carboxylic acid side…

A:

Q: What is the conjugated base of this equation?

A:

Q: Give product and iupac name

A:

Q: What is the final product

A: LiAlH4 reduce the acid to form alcohol which was then attack with the carbonyl group form the…

Q: Draw the reaction between methyl-2-octynoate and cysteine with electron pushing. this is Michael…

A: below answer is given

Q: The organic product of this reaction is

A:

Q: explain the process named as Ozonolysis with example.

A:

Q: what is the plausible synthesis?

A:

Q: complete

A: We will write the reaction conversion

Q: complete the following synthesis produces using a proper reagent and products

A: Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional…

Q: What will the formula be of the main produc

A: Answer is there is formation of ether  CH3OCH2CH2CH3

Q: Question attached

A: Given reactions:

Q: What for you mean by Nucleophilic Substitution ?

A: Nucleophiles are those elements or compounds which are electron rich. These have lone pair of…

Q: Give major product part a,b,c properly

A: Solution- major product of given below with there reaction;

Q: product formed in this reaction.

A: Alcohols:  It's general functional group is R-OH Alcohols upon heating in presence of acid, it…

Q: Draw the Wittig reaction mechanism with arrow pushing.

A: Wittig reactions are helpful in alkene synthesis using aldehyde/ketones on treating with triphenyl…

Q: the principal product of the following reaction

A:

Q: What type of carbocation is shown?

A: As we can clearly see that the positive charge (cation) containing carbon is attached to two carbon…

Q: for this reaction scheme suggest a reagent that could be used to accomplish the first step and draw…

A: Alcohols on reaction with sodium metal forms sodium alkoxide . R-OH + Na ------> R-O-Na+ Sodium…

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.