Give all answer.i will rating you с.Shown below is a N-glycoside formation giving a major and a minor product.онононноноHOноH.ноноOHOHHN(i) Identify the reagents and reactants used to give B and C.(ii) Discuss the mechanism of the reaction leading to B and C.(iii) Identify the major product. Briefly justify your answer.

1. Reactant ( beta D-glucose + aniline ) in presence of acetic acid. 2 .Mechanism a. first…

Answered: (i) Identify the reagents and reactants…

(i) Identify the reagents and reactants used to give B and C. (ii) Discuss the mechanism of the reaction leading to B and C. (iii) Identify the major product. Briefly justify your answer.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter10: Organohalides

Section10.SE: Something Extra

Problem 19MP: The formation of Br2 from NBS first involves the reaction of NBS with HBr to form an iminol...

See similar textbooks

Related questions

Q: Write the reaction mechanism between ethane and chlorine in the presence of light. Label each step…

A: To find: the reaction mechanism between ethane and chlorine in the presence of light.

Q: The reaction that occurs when the benzaldehyde you have is reacted in a basic environment is called…

Q: ) Answer the following questions regarding solvent polarity and reaction rates. i. Suggest how to…

A: Transition state can be defined as the state where new bonds are formed and old bonds are broken.

Q: Write the mechanism and predict the product for the reaction of cyclohexene with bromine. Make sure…

A: Cyclohexene reacts with bromine to make 1,2-dibromocyclohexane.

Q: write the free radical monosubtitution mechanism for the bromination of ethane to produce…

A: - We have to calculate a bromination of ethane of produced bromoethane to free radical…

Q: Write the mechanism and predict the product for the reaction of cyclohexene with bromine.make sure…

A: Halogenation is a reaction to the addition of halogen in unsaturated alkene and alkynes.…

Q: write the complete reaction mechanism between ethylbromide (using steps and arrows ) and NaOH and…

Q: Homogeneous catalytic hydrogenation of the compound below gives two isomers of the same product.…

Q: CI Cl, / CH,CI, НО

A: The organic compounds in which a C=C bond is present are known as alkenes. Alkenes undergo an…

Q: Draw/outline a reasonable and detailed mechanism for the dehydration of 2-methylcyclohexanol…

Q: Provide the structure of the product and write the mechanism of its formation for the following…

A: Given two reaction are of intermediate chemistry i.e. carbocation formation reaction. Reactive…

Q: Although useful in agriculture as a soil fumigant, methyl bromide is an ozone-depleting chemical,…

A: The mechanism for the formation of methyl bromide from methanol and hydrogen bromide has to be given…

Q: Give the condensed structure of the product/s for the reactions below and indicate for each the…

Q: Under milder temperatures than what is needed for dehydration, strong acids catalyze the…

A: `The formation of di-n-propyl ether from 1-propyl alcohol under strong acidic conditions is a…

Q: Outline a mechanism for the dehydration of 2-methylcyclohexanol catalyzed by phosphoric acid.…

A: Mechanism : Dehydration of alcohol under acidic condition follows E1 reaction mechanism. It is…

Q: Write equations that show the mechanism of the dehydration of 3-pentanol. Two possible products can…

A: Dehydration is done using concentrated sulfuric Acid which can Remove water from the molecule .

Q: H,SO, OH

A: Protonation Loss of leaving group Deprotonation

Q: Outline a mechanism for the dehydration of 2-methylcyclohexanol catalyzed by phosphoric acid.…

Q: Which group of side chains is most likely to take part in the catalysis during an enzymatic…

A: The solution of the question is given below:

Q: (b) Provide Following : the mechanisms of the fy Hoffmann-Loffier reaction (ü) Miyamura reaction

Q: Write an equation(s) to illustrate the mechanism for the dehydrohalogenation of…

A: Concerted means the bond breaking and bond forming process takes place simultaneously.

Q: Explain and describe details for this mechanism.

A: Acid protonated the carbonyl oxygen and makes it electrophilic or increases ots electrophilicity

Q: (a) Consider the reaction of HBr with 1-butene and 2-butene, Identify the one which will follow…

A: In organic chemistry, inter conversion of organic molecule takes place from one form to another form…

Q: When exactly 1 mole of methane is mixed with exactly 1 mole of chlorine and light is shone on the…

Q: Please prepare a mechanism for the conversion of ethane and chlorine gas to ethyl chloride and…

A: Substitution reaction for ethane and chlorine.

Q: Two organic compounds D and F with molecular formula C4H9Br react with suitable reagents to form E…

A: SN1 - Unimolecular nucleophilic substitution reaction The SN1 reaction involves two steps The…

Q: P.

A: The above reaction driving force is increase in entropy.One molecule of aryl alkyl bromide gives…

Q: (a) suggest the suitable mechanism and illustrate the stepwise of the (heptyloxy)cyclopentane…

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Write and explain the mechanism in the reaction.

A: Alkene gives an electrophilic addition reaction with hydrogen halide. The reaction proceeds in two…

Q: . (a) A substitution reaction occurs when 2-bromopropane reacts with aqueous sodium hydroxide. (i)…

Q: Predict the products of reactions of carboxylic acids with alcohols, amines, diazomethane,reducing…

A: Since you have posted multiple questions and have not specified which part you want us to solve, we…

Q: Ozonolysis process was carried out towards an unknown organic compound, X, to produce propanal,…

Q: Please provide a step by step list explaining the mechanism for the reactions

Q: Present a synthetic route reported in the literature for the synthesis of the captopril from…

A: Introduction: Captopril is a drug used for hypertension and heart failure. Basically it is an…

Q: When cyclohexanol is dehydrated to cyclohexene, a gummy green substance forms onthe bottom of the…

A: Cyclohexene is prepared on dehydration of cyclohexanol using acid catalysts like phosphoric acid.…

Q: give the mechanism of the following reactions and explain why any selectivities occur.

A: The reaction taking place is given as,

Q: Et CH,OH, H* H2. Ni Raney H,0, H* Me Chauffage Me

Q: Complete the following reaction and provide a detailed, step-by-step mechanism for the process. HBr

A: It is an SN1 reaction. This reaction based on a more stable carbocation intermediate. First, alkene…

Q: a. Complete the following reactions and outline the mechanism for the formation of the product: CH,…

A: Alcohols when treated with Halogen acid then results in formation of alkyl Halides. Tertiary…

Q: Q2. Outline the possible reaction pathways with propose mechanism for the formation of Nylon 6 from…

A: Polymer can be defined as the chemical compound that is formed by the combination of one or more…

Q: Elucidate the structure, hybridization, stability order and factors affecting the stability of an…

A: Free radical is also known as radical. Which contain only one unpaired electron.

Q: Write the product of the following reaction. Indicate the mechanism of the reaction involved.

A: A question based on Gilmann reaction, which is to be accomplished.

Q: Provide the mechanisms for chlorination of toluene which include the initiation, propagation and…

A: The mechanism for the chlorination of toluene has to be given. The structure of toluene is given…

Q: State whether the reaction below gave a single product or more than one product in quantities…

A: Ethers are a class of organic compounds where an oxygen atom is connected to two alkyl or aryl…

Q: Draw the reaction mechanism of conversion of compound 4a to 4b. Indicate what type of reaction…

Q: (c) Outline the mechanism for the bromination of 3-methylcyclobutene.

Q: 1. Provide the structure of the product and write the mechanism of its formation for the following…

A: Reaction d and f are pinacol and semipinacol rearrangement respectively. Pinacol-pinacolone…

Concept explainers

Analyzing and Predicting Spectroscopic Data

The interaction of electromagnetic radiation with the structure of molecules in the sample and their study is referred spectroscopy. Several spectroscopic methods are used to acquire sample information, and these methods are proved to be accurate, fast, and non-destructive. The information obtained about the content and composition of molecules from these spectroscopic methods is called spectroscopic data.

Question

100%

Give all answer.i will rating you

с.
Shown below is a N-glycoside formation giving a major and a minor product.
он
он
он
но
но
HO
но
H.
но
но
OH
OH
HN
(i) Identify the reagents and reactants used to give B and C.
(ii) Discuss the mechanism of the reaction leading to B and C.
(iii) Identify the major product. Briefly justify your answer.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step by step

Solved in 2 steps with 2 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Analyzing and Predicting Spectroscopic Data

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

(0) Identify and show the mechanism to form product A and B ço,CH, acid hydrolysis ČO,CH3 B.
Like acid chlorides, acid anhydrides react with alcohols in the presence of pyridine to form esters. For the following reaction : (a) Draw a circle around the nucleophile ; (b) Draw a square around the electrophile; (c) Put a star next to the base; (d) Draw the structure of the tetrahedral intermediate in the box below. Then draw a reasonable 3-step arrow pushing mechanism for the reaction.
2. For the reaction scheme below: (i) Suggest a reagent X that could be used to accomplish the first step. (ii) Draw the curly arrow mechanism for the second step in the scheme. он Na
Provide the complete mechanism using CAF for the reaction of aniline sequentially with (i) acetic anhydride, (ii) nitronium ion; (iii) aqueous base. Name the final product(s) formed.
Q3. Consider the ring closing metathesis (RCM) sequence used for the synthesis of macrocycle E and answer Parts (a) and (b). E F HO OH G H (a) How could you convert unsaturated ester F into E (two steps are required, give conditions/reagents but not mechanisms)? (b) Disconnect ester F, showing the synthons to lead to equivalents G and H. Give the conditions for the forward synthesis
3) While we expect to get one major product, this reaction could potentially have some issues with formation of multiple products. What is the relationship between the two major products that you might expect for the reaction of E-stilbene and dimethyl fumarate? Why will this not matter when you look at the NMR? 4) In addition to the issue raised in prelab Q3, 2,3-dihydrofuran and styrene will also give give two additional major products – what is their relationship, and will this matter when you look at the NMR?
3) While we expect to get one major product, this reaction could potentially have some issues with formation of multiple products. What is the relationship between the two major products that you might expect for the reaction of E-stilbene and dimethyl fumarate? Why will this not matter when you look at the NMR? 4) In addition to the issue raised in prelab Q3, 2,3-dihydrofuran and styrene will also give give two additional major products - what is their relationship, and will this matter when you look at the NMR?
The reaction that occurs when the benzaldehyde you have is reacted in a basic environment is called the Cannizzaro reaction, and when it is reacted with cyanide, it is called benzoin. Write down the reaction mechanisms of these reactions and explain why.
2. Some steps of the total synthesis of Sativene are shown below. (a) For each step indicated, identify the functional group transformation (FGT) on the line below the arrow, and provide reagents that will accomplish this transformation above the arrow. R но, FGT: 2 FGT: H2SO4 R FGT: (b) Draw the mechanism of the transformation of 2 to 3, AND draw the mechanism of 3 to 4.
3. Treatment of 1-phenyl-2-propenone with a strong base such as LDA does not yield an anion, even though it contains a hydrogen on the carbon atom next to the carbonyl group. Explain. (a) Ethyl pentanoate H Ethyl 2-methylbutanoate CH₂ . Which of the following compounds can be prepared by a malonic ester synthesis? Show the alkyl halide you would use in each case. 1-Phenyl-2-propenone (b) Ethyl 3-methylbutanoate (d) Ethyl 2,2-dimethylpropanoate
This question is related to the aldol reaction of carbonyl compounds depicted below. NH₂ NH₂ h OH (a) Draw a reaction mechanism for this reaction (b) Identify which of these compounds are chiral and draw the hashed-wedge structures of them around each chiral atom (c) Provide the Cahn-Ingold-Prelog (CIL) identifiers for the chiral compounds identified in (d) Provide the IUPAC name of each of the three compounds (e) Compound C can undergo a subsequent reaction to yield the a,ß-unsaturated product. Draw and name the product of this subsequent reaction (f) Draw a mechanism for the subsequent reaction to form the a,ß-unsaturated product
b) In order to synthesis 1-phenylbutan-1-ol, you started the reaction with a hydration of prop-1-ene using the hydroboration method. Then you oxidized the intermediate with KMNO4. Finally, alkylation using C6HSMGB was performed to obtain the final product. However, the reaction was not successful. Analyse the reaction by explaining what happened to the reaction and provide the correct synthetic method.