b. Br OCH3 d. CHз Он a. e. C. "OCH3

Q: What will be the major product for the following reaction?

A: Carboxylic acid react with alcohol form ester

Q: Q5. What product is formed when cyclohexanone is reacted with each of the following reagents? MgBr…

A: We have to predict product of reactions.

Q: What are the products formed from the following reactions:  1) The addition of dimethylborane…

A: Dimethylborane (DMB or Me2BH) is a chemical reagent that is used in organic synthesis as a source of…

Q: 애

A: Instion of bromine to alkyl chain via HBR .by the treatment with H2O it convert into primary alcohol…

Q: Which of the following sequences of reactions would convert toluene to 2-bromo-4-cyanotoluene? ? Br…

A: At first nitration gives 4 Nitro toluene. Then bromination gives 2 bromo 4 Nitro toluene. Then…

Q: Show how the following compound can be synthesized from an alkene. = OH CI

A:

Q: How is trans-2-methylcyclohexanol prepared from 1-bromo-1-methylcyclohexane?

A: Given reactant is 1-bromo-1-methylcyclohexane and the product is 2-methylcyclohexanol. In order to…

Q: What is(are) the major product(s) of the following reacti HC1 H;C OH

A: We will get two products

Q: 16-64 How would you synthesize the following substances starting from benzene? (a) CI (b) HOCH2…

A:

Q: Na2CO3, H2O N. NH2

A:

Q: Using cyclohexanone as the starting material, describe how the following compounds can be…

A: In this conversion, Cyclohexanone will be reacted with NaBH4 + H3O+ which forms cyclohexanol. Then,…

Q: What are the reagents of the following reaction? он но

A: Three member cyclic epoxide is very reactive, so I can used acid as well as base for the ring…

Q: a) How would you synthesize the following compounds from cyclohexanone? b) CO,H

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: - What is the major products formed when benzene reacts with the following : 1-…

A: Major product of following reactions: 1)chloro-2,2-dimethyl propane + benzene ----> ? 2) fuming…

Q: Answers to Question: How would you prepare the target product from benzene? It takes more than two…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Treatment of 3-methylcyclohexene with HCl yields two products, 1-chloro-3methylcyclohexane and…

A: When 3-methylcyclohexene is treated with HCl to give 1-chloro-3-methylcyclohexane and…

Q: cyclohexylethyl ether CH;CH,Br Br CH;CH,O

A: Given, Below are two possible means of synthesizing the following compound, cyclohexyl ethyl ether.…

Q: Benzene undergoes electrophilic aromatic substitution reaction with alkyl halide in the presence of…

A: Benzene undergoes electrophilic aromatic substitution reactions with alkyl halide in the presence of…

Q: Provide the major product for the reaction of the following starting material with excess HBr. If…

A: Markovnikov's rule:  When an unsymmetrical reagent is added to unsymmetrical alkyne the negative…

Q: Start from 2-methylcyclohexanol and show the steps and mechanisms for the following products.…

A: Alkenes are synthesized from alcohol by the dehydration of the alcohol. This reaction is acid…

Q: How would you synthesize the following substances startting from benzene (a) (b) „CH3OH „CH;CH;OH…

A: a)First step is the Friedel craft alkylation which is then treated with NBS reagent. After the…

Q: The major product from the dehydration of 2,3-dimethylcyclohexanol with H2SO4 catalyst is O…

A:

Q: HO HC=CH

A: From acetyle The given compound have to synthesize .

Q: 9) How would you carry out the following transformation? More than one step may be required, write…

A: Given are organic synthesis reactions.In first reaction alkene is converted into trans diol…

Q: Using bromocyclohexane as a starting material, how could you synthesize the following compound?

A: Bromocyclohexane is treated with magnesium and ether to form cyclohexylmagnesium bromide and it is…

Q: Which of the following is the product for the given reaction? HNO3 ? H2SO4

A:

Q: How would you synthesize propane from propanone? Provide a mechanism.

A: We have to predict the mechanism for the synthesis of propane from propanone.

Q: Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: 2) How would you synthesize the following compounds from cyclohexanone?: a) b) CO₂H

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Provide reactants, reagents, and/or products for the followin NH2 + H

A: Reactants: benzaldehyde and phenylamineReagents: ethanol (5M) at room temperatureProducts:…

Q: A) B) H3CO `ОН + 1. Na Br CN Ű÷ A cn H

A:

Q: Acetylene reacts with sodium amide in the presence of propyl halide

A:

Q: Provide the major product for the reaction of the following starting material with H2O, H+. If more…

A:

Q: Synthesize the following compounds from the indicated starting material. OH a) Br Ph OH b) Br CHCH3…

A: Given first two product we can get by grignard addition reaction. And last can be get by elimination…

Q: Draw the resonance structure of the following intermediates in the nitration of phenol: OH =

A: The Resonance  structure  are as follows.

Q: Draw the products formed when the following alkynes are treated with each set of reagents: [1] H2O,…

A: (a) In the given reaction a terminal alkyne, 4-methylpent-1-yne reacts with H2O, H2SO4 (strong acid)…

Q: In a strongly acidic solution, cyclohexa-1,4-diene tautomerizes to cyclohexa-1,3-diene.Propose a…

A:

Q: 11b) Synthesize the following: CI OH

A: In this synthesize process primary amin reaction with carboxylic group to produce amide group then…

Q: How do you synthesize a cyclohexane-1,2,3-triol from a cyclohexane

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.