which react faster and slower than benzene; bromobenzene, benzonitrile, benzoic acid, nitrobenzene, benzenesulfonic acid, or methoxybenzene?

Q: Outline syntheses of each compound and any other required reagents.

A: Alcohol is oxidised to give aldehyde and carboxylic acids.

Q: Why does water have a retarding effect on the nitration ? e) Explain why Benzene has lower…

A: addition of NO2 + (electrophile) from HNO3 to aromatic compound  is known as nitration,

Q: From 1 being the slowest and 4 being the fastest rank the aromatic hydrocarbons in terms of…

A: The compounds given are,

Q: Which of the following dihalides is/are an appropriate substrate, when treated with a strong base…

A: To solve this problem we have to convert dihalides into  an alkyne .

Q: Where will a nucleophile initially bond to the structure of carvone, provide a reason

A:

Q: Choose the best answer. Which of the following has similar preferred site ( carbon #) for…

A: The solution of the question is given below:

Q: HI (excess)

A: While writing the mechanism use electron pushing arrow from electron rich center to electron poor…

Q: Explain how Hammond's postulate accounts for the higher selectivity of bromination reactions as…

A: We have to explain how the Hammond postulate accounts for the higher selectivity of bromination…

Q: Explain in details the mechanism of preparing B-ionone from first step till last step. Please write…

A: Applying concept of organic synthesis and reagent.

Q: Which of the following could act as an electrophile?

A: Answer: b.H3O+  (hydronium ion)  Explanation: Electron pair acceptor (or) electron deficeint (or)…

Q: What is product E, and draw the structure

A:

Q: Rank the following species from best nucleophile to poorest nucleophile in an aqueous solution (in…

A: Given that : We have to rank the following species form the best to the poorest nucleophile in…

Q: ОН HO (a) (b)

A: Detail synthetic scheme is shown below for both compounds

Q: tow is benzophenone suited for nueleophilie aromaic abstitution Which positions and the be…

A:

Q: c. Describe (using appropriate figures) one reaction that exploits epoxides as the starting…

A:

Q: Which reacts fastest & slowest with m-chloroperbenzoic acid, why?

A: We know that   The mCPBA is peroxy acid it react with alkene to form epoxide.  the electrophilic…

Q: Which reagents could be combined to make the following in a reasonable number of steps and order?

A: To determine which reagents could be combined to make below compound

Q: Provide the curved-arrow mechanism to account for the following nucleophillic addition-elimination…

A:

Q: Compare the acidity of ammonia and its aliphatic derivatives with of acidity pyrrole?

A: The lone pair on the nitrogen atom present in a compound is responsible for the basic character of…

Q: synthesize the above, respectively, starting with Se8.

A: The gain of electron is named as oxidation whereas loss of electron named as reduction. The reaction…

Q: Is a intramolecular Friedel Crafts acylation reaction. As you from the product, the acylation…

A: Applying concept of organic synthesis and reagent.

Q: Why does bromination give exclusively anti products while chlorination gives a mixture of syn and…

A: Halogenation is the addition of halogens to alkenes. Halogenation usually gives anti products. If…

Q: List down the following safety guidlines by doing the heat of reaction experiment:

A: 1)Always wear safety glasses 2)always point the test tube away from any other person in the lab.…

Q: Please Complete the following reaction with Major Compund with explaination in handwritten....

A:

Q: Which will react slower in polar protic solvents

A: Polar protic solvent is polar solvent.

Q: Why witting reaction is more suitable for making alkene as compared to other methods of preparation…

A:

Q: Provide the missing reagent indicated by "???" CI ??? OH (+ other products)

A: Nucleophilic reactions are identified as of two types namely substitution and elimination. In the…

Q: What would the major organic product of the first step of the reaction in the question be if the…

A: Given reactants are acid chloride and aniline. If we add AlCl3 to this reaction then this reaction…

Q: Propose mechanism consistent with the following reactions a and b.

A: Since we know that HBr react with alkene in presence of peroxide by radical mechanism and follow…

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: Arrange the following compounds according to their rate of solvolysis with suitable explanation.

A: SN1 reaction: SN1 stands for nucleophilic substitution first order, where the rate of reaction is…

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A: Given compounds,

Q: OMe

A: The product has a cyclopropane ring in place of double bond of 1st substrate. The double bonded…

Q: Reaction of with CH3CH₂COOH forms CH3CH2CH2OH as a product. O NaBH4 O HCI O LiAlH4 O CH3NH2 O KMnO4

A: Given,  Reaction of ...............with CH3CH2COOH forms CH3CH2CH2OH as a product.  Fill the blank ?…

Q: 1.

A: Reaction 1 : Acid catalyzed esterification. Reaction 2 : C- acylation.

Q: Indicate the true electrophile that Aromatic Ring in Nitratien

A: Nitration is a process by which a nitro group is added to an organic compound. Here, the organic…

Q: Ph

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: Write down the reduction reaction of each molecule using appropriate reagents, listing the follo…

A: Since you have posted multiple parts, the answer for first three parts are given below. Kindly…

Q: Benzoyl chloride undergoes nucleophilic substitution at a faster rate than methyl propanoate because

A: Nucleophilic attacks on both benzoyl chloride and methyl propanoate are examples of nucleophilic…

Q: her question will stve this respo on 18 Which aly chioride reacts fastest in S2 reactions?

A: The SN2 reacction is most favored in those alkyl halides which forms less stable carbocation.…

Q: Give the major organic product for each step of the following reaction

A:

Q: Order of reactivity towards nucleophilic substitution reaction of the compounds

A: Order of the reactivity towards nucleophillic substitution reaction of the compound

Q: De most common method for the synthesis of unsymmetrical ethers is the Williamson synthesis, a…

A: The complete synthesis of 2-propoxypropane from propene is show below, The acid catalyzed hydration…

Q: By what mechanism is the following reaction likely to occur? (SN1, SN2, E1, E2) Put an "and" between…

A: In 1 reaction alkyl halide is 1°and SH- is strong nucleophile. SN2 reaction will takes place.…