Decreasing order of electrophilic substitution reaction for the given compounds is

Q: Predict the initial and isolated products for the reaction. Hint: the products are isomers and in…

A: Alkynes are the organic compounds which contain one or more triple bonds in it. These compounds…

Q: Compare the following pairs of molecules and determine which one is the stronger nucleophile

A:

Q: Find the major organic product of the given reaction.

A: Three membered rings formed by two carbon and one oxygen atom is known as epoxide ring. The…

Q: at is the correct order of decreasing reactivity ost reactive first) of these compounds toward…

A: When electron donating groups are attached to benzene ring.so, they increase the reactivity towards…

Q: Which of the following species cannot be considered a nucleophile?

A: A. Carbocation is electron deficient. Therefore it act as electrophile. B Oxygen is having lone…

Q: This is a hydrogenation and carbene addition problem. How do I draw the structure of the major…

A: The carbene addition reaction keeps the stereochemistry of alkene.

Q: Which of the following is/are not feasible for the following ether synthesis?

A: Answers are explained Below

Q: šive the product of the bimolecular elimination from each of the isomeric halogenated compounds.

A: The reaction in which two atoms leave a substrate molecule and a double bond is formed in the…

Q: In an electrophilic aromatic substitution, the substitution pattern on the product is determine by…

A: A nucleophilic aromatic substitution reaction is a organic reaction. In which the nucleophile

Q: PLEASE SELECT ONLY 1 OPTION FROM THE FOLLOWING ONLY OPTIONS:     Elimination 2nd order Radical…

A: Diels-Alder reaction: The Diels–Alder reaction is a reaction between a conjugated diene and a…

Q: er sphere mechanism for

A: Coordination compounds undergo the redox reaction by two kinds of mechanisms. If the transfer of…

Q: Show all the steps necessay,in order to make each of the followring compoundS, Starting with benzene…

A: Preparation of 2,4-Dibromobenzoic acid from benzene can be done as follows:

Q: What will be the optical conformation of the product in the following reaction?

A:

Q: What is/are the major productis) of the following reaction?

A: Formation of 3-membered cyclochloronium ring intermediate is formed in the first step.  In the next…

Q: This is a hydrogenation and carbene addition problem. How do I draw the structure of the major…

A: Interpretation: We have to write the product for the following reaction.

Q: Increasing alkyl substitution stabilizes an alkene by an electrondonatinginductive effect. Explain ?

A: Alkene are hydrocarbon having carbon - carbon double bond . Increasing alkyl substituents ,…

Q: alkyl halide is most likely to A undergo the which forms a carbocation intermediate. reaction…

A: There are basically two types of substitution reactions ;-  SN1 (nuclephilic substitution…

Q: synthesize the

A: Dear student this question is related to the organic chemistry.

Q: Which of the following is most likely to be the first step in the general mechanism for…

A:

Q: An α carbon of a ketone or aldehyde can be alkylated or halogenated under basic conditions. Recall…

A: In the alpha halogenation reaction, an enolate formed from an aldehyde or ketone reacts with a…

Q: Which of the following is the rate- determining step in the electrophilic aromatic substitution of…

A: In Electrophilic aromatic substitution of benzene an electrophile replaces the hydrogen atom present…

Q: The electrostatic potential maps of benzene and pyrrole are shown here. Is the electrostatic…

A: The red color in the electrostatic potential map represents the high electron density or an…

Q: Which of the following species cannot be considered an electrophile?

A: Electrophile is neutral or positively charged species. Nucleophile is neutral or negatively charged…

Q: mechanism for the of hydrolysis (1-bromo of Propose a reaction methylpropyl)cyclohexane. Including…

A: Stereochemistry is branch of chemistry in which we deal with arrangement of atoms in three…

Q: How can you distinguish in a SNAr reaction whether it will occur according to an addition-…

A: Nucleophilic substitution reactions on aromatic compounds can occur in two ways.

Q: which

A: Nucleophilic substitution reaction in which an nucleophile substitute any group from reactant.

Q: Decide which compound in pair is more reactive in electrophilic aromatic substitution reaction…

A: In electrophilic substitution reaction benzene reacts acts as nucleophile . So compound which have…

Q: Give two possible [1,2]-rearrangement products where an alkyl group migrates in the following…

A: Organic reaction mechanisms:

Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.

A: The intermediate of the given reaction is a carbocation. In carbocation, carbon carries a positive…

Q: What alkene yields attached set of oxidative cleavage products ?

A: What alkene yields an attached set of oxidative cleavage products has to be determined.

Q: The following carbocation undergoes a rearrangement by a hydride shift as shown below. The reason…

A: Given, a carbocation which undergoes rearrangement by hydride shift  We need to explain the reason…

Q: The reaction shown here is called the pinacol rearrangement. A carbocation rearrangement is believed…

A: When vicinal diols are treated with acids, they can be rearranged to give aldehydes or ketones. This…

Q: Which of the following is the correct order of increasing reactivity in nucleophilic substitution…

A: Acid halides, esters , anhydrides, amides etc. are the carboxylic acid derivatives. Their reactivity…

Q: How many different products obtained upon ozonolysis of are ?compound A

A: unsaturated compounds (alkynes,alkenes etc)  reacts with ozone to form carbonyl compounds ,.…

Q: Predict the Mechanism which will inform stereo and regioselectivity on table given. Answer on…

A: The following mechanism and the bases and electrophile will be mentioned in a list given below. Also…

Q: In both series below the three aromatic compounds illustrated undergo the electrophilic substitution…

A:

Q: Explain why substitution is difficult on accomplish on the benzene ring?

A: Benzene is a planar molecule having delocalized electrons above and below the plane of ring. Hence,…

Q: Predict the main product of each of the following reactions with their

A: a. alpha hydrogen containing aldehydes or ketone in presence of base to give aldol first, further…

Q: please explain what happens in this reaction mechanism. be as DETAILED as possible. acetylene +…

A: Br2 is a covalent compound, there is no charge separation. But during the reaction there is a…

Q: Because they are so often used as protecting groups in organic synthesis, the choice of which acetal…

A:

Q: Which statement(s) is(are) true concerning the rate-limiting step involving the benzene ring? CI…

A: The given above reaction is an example of Friedel Craft reaction.In presence of anhydrous AlCl3 and…

Q: The following compounds are capable of degenerate rearrangement at the temperature given. Identify…

A: The given compound is capable of degenerate rearrangement at high temperature.

Q: Which will react faster??

A: Sn2 reaction is  bimolecular nucleophilic substitution reaction

Q: nvestigate what happens when an alkene reacts with potassium permanganate as well as when it reacts…

A: Potassium permanganate is an oxidising agent hence under acidic or basic condition when reacts with…

Q: For the following carbocation determine if it is likely to rearrange, and it so, select the correct…

A:

Q: How many transition state/s is/are present in the reaction based from the energy diagram as shown…

A: Given is energy diagram.

Q: Draw all the different monochlorinated products one would be by the radical chlorination of…

A: Free radical halogenation is basically a type of reaction which substitutes a chlorine or bromine…

Q: Draw both resonance structures of the most stable carbonation intermediate in the reaction shown…

A: No alpha hydrogen increases the stability of carbocation increases.

Q: For each of the following reactions draw the structure of the major organic product in the box…

A: Hello. Since the question contains multiple sub-parts, the first three sub-parts shall be solved…

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.