What compound is the major product of the reaction sequence shown below?(1) KCN ethanolОн(A)NH2(B)(2) LIAIH, (xS)/ether(3) dil. H* H;OонNH2OH(C)(D)Compound CCompound D)Compound AO Compound B

The reaction with mechanism is as below :-

What compound is the major product of the reaction sequence shown below? (1) KCN, ethanol OH (A) NH2 (B) (2) LIAIH, (xS)/ether (3) dil. H* H20 он он (C) (D) Compound C Compound D Compound A Compound B

What compound is the major product of the reaction sequence shown below? (1) KCN, ethanol OH (A) NH2 (B) (2) LIAIH, (xS)/ether (3) dil. H* H20 он он (C) (D) Compound C Compound D Compound A Compound B

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter24: Amines And Heterocycles

Section24.SE: Something Extra

Problem 31MP: Predict the product(s) and provide the complete mechanism for each reaction below.

See similar textbooks

Related questions

Q: 6. Provide a step-wise synthesis for the following compound from starting material. Be sure to show…

Q: Q17. Compound 1 can undergo an intramolecular reaction to give cyclic product 2. Using curly arrows,…

A: Cyclic product is formed , which is cyclic amide , ester functional group act as electrophile and…

Q: Choose the right reagent from the pool to carry out the following reactions. ( KMN04, H2CRO4, NABH4,…

A: The solution is given below -

Q: The compound eutypine is an antibacterial agent isolated from the fungus Eutypa lata. This fungus…

A: In question it has been given that the eutypine has to be formed from a given reactant along with…

Q: Provide the appropriate reagents or product in the following examples. 1. Me он Me Me Me 2. 1. NaBH,…

A: Since you have asked multiple questions we can answer the first three for you. To get the remaining…

Q: Which compound shows the highest rate of reaction when shaken vigorously with ethanolic silver…

Q: Predict the major product of the following reaction sequence. 1) BH3-THF ? 2) Н,О,, NaOH Br OH There…

Q: Give the major organic product(s) of the following reactions (a-e).

Q: Provide the major organic product of the following reaction sequence. 1. NAOCH2CH3 .Co,CH2CH3 2.…

Q: When allyl bromide is refluxed with magnesium metal in ether solvent, the product formed is…

A: At first grignard reagent is formed, and it become nucleophilic, so further attack in allyl bromide…

Q: H2O, H-SO4 1. NaNH2, NH, 2. CH,CH,Br Compound E Compound F

Q: Muscalure, the sex pheromone of the common housefly, can be prepared by a reaction sequence that…

A: The formation of A and B in the reaction are shown below.

Q: Decytospolides A and Bare fungal natural products that are toxic to some cancer cells, In a…

A: Concept : 1) NaH is used as base for deprotonation. 2) Grignard reagent is used as nucleophile here…

Q: (b) State the reagents needed to convert benzoic acid into the following compounds. (i) C6H§COCI…

A: In organic chemistry, the inter conversion of organic molecule takes place by the help of various…

Q: O,N. Br O2N

Q: Predict the product formed when the compound shown below undergoes a reaction in the presence of…

A: The product of the above transformation is given below

Q: Propose a synthesis of the compound shown below starting with benzene and any other acydic carbon…

Q: The Claisen condensation of two molecules of ethyl phenylacetate (shown below) in the presence of…

Q: 1.Provide the identity of Intermediate I and Intermediate Il in the following synthetic sequence,…

Q: D. Provide reasonable mechanisms for the following reaction H NaOH, H₂O, A

A: Aldol condensation: The alpha hydrogen of carbonyl compounds is acidic in nature and it is removed…

Q: c) Write a detailed mechanism for the following transformation: OH CH;OH H,SO, (cat)

Q: Give the structure of compounds A to E in the following reaction sequence.

Q: 2H2/Pt в "NH2 CH3Br - A H3C-CECH C

A: Given incomplete reaction is : Give the major products = ?

Q: NO2 HBF4 Br, FeBra H2, Ni NANO2, H0*

A: We have to predict the major product from the given reagents.

Q: Which of the following is most prone to hydration (acid-catalyzed reaction with water)? a. b. C. d.…

A: Aldehyde which is most prone to hydration is.

Q: Identify reagents that can be used to achieve the following transformation: OH O 1) NaOH, 2) RCO3H,…

Q: 21.(4) Provide a mechanism for the following transformation. кон heat Br

A: ->KOH is a base which can substrate Hydrogen and give elimination reaction.

Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. H-A H2N HO HAN

Q: The (+) - aureol is a natural product that has shown selective activity against certain colon and…

A: Carbocations rearrange to produce more stable carbocations. In the rearrangement of carbocation, the…

Q: Q17. Compound 1 can undergo an intramolecular reaction to give cyclic product 2. Using curly arrows,…

A: Applying concept of cyclation reaction of formation of cycloamide.

Q: 2b. Device a synthesis route for the following: Hg(OAc): NaBH, он p-TSCI pyridine a) b) KCN d)

A: Oxymercuration reaction: The alkene gives an electrophilic addition reaction to form alcohol. When…

Q: What is the configuration of the chiral center in the bromoepoxide? How do you account for the…

A: Step 1- Is a Fischer esterification to make diethyl malonate. Step 2-Protectionhydroxyl group in the…

Q: 2. Give the structures of compounds A and B in the following reaction scheme. 'N OMe 1. ОН /Н20 1.…

A: The reagent sodium dichromate (Na2Cr2O7) works as the oxidizing reagent. It basically oxidizes…

Q: The compound below can undergo E2 reaction mechanism upon addition of sodium chloride. F Select one:…

A: Elimination reaction of alkyl halide: Alkyl halide gives an elimination reaction by reacting with a…

Q: Compound that will Positive Differentiating Chemical test sign/s of reaction Compound A Compound B…

Q: The compound to the right was treated under the following two conditions. Give the major product(s)…

A: a) Left at room temperature overnight in ethanol favors sn1 mechanism. b) Refluxed in boiling…

Q: 1. Draw the retrosynthetic analysis of compound A by providing the appropriate disconnection and…

A: We have to suggest a complete synthetic pathway with the reagents and reaction conditions to…

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H20 + МеОн HO, OMe cat.…

Q: Compound that will Positive Differentiating Chemical test sign/s of reaction Compound A Compound B…

Q: А B C D Br Br

A: We have to rank the order of the reactivity for the given compound

Q: In the lab, you are provided with an unknown C, which when reacted with O3 followed by (CH3)2S…

Q: Select the expected product of the following reaction sequence. NaCN 1. LIAIH, THF DMSO 2. Hао Br…

A: For the given reaction in the first step SN2 reaction take place to form alkyl cyanide with…

Q: Provide a plausible curved-arrow mechanism for the following transformation. سلاح 1) NaOEt, EtOH 2)…

A: This reaction mechanism follows the reverse process of Claisen ester condensation.

Q: 3. Draw a detailed reaction coordinate diagram. 4. Provide transition state drawings for each step…

A: The presence of R-O-R' linkage in a molecule is termed as the ether linkage, where R and R' can be…

Q: Give the relative rates of reaction of propyl acetate with the four reagents below to give a…

A: Reactivity depends on the polarity of bonds. The higher the polarity, the more will be the…

Q: 2. Propose a reasonable mechanism, using curved arrow notation, for the following transformation.…

Q: Give the product for the following reaction CH3 OH CH3 H₂SO4/PCC → (a) (b) (c) (d) CH3 CH3 CH3- CH3…

A: Organic reactions are those in which organic reactant react to form organic products. H2SO4/PCC is…

Question

What compound is the major product of the reaction sequence shown below?
(1) KCN ethanol
Он
(A)
NH2
(B)
(2) LIAIH, (xS)/ether
(3) dil. H* H;O
он
NH2
OH
(C)
(D)
Compound C
Compound D
)Compound A
O Compound B

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 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Selection Rules for Pericyclic Reactions

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

The major organic product in the reaction sequence below is:
a. Identify the two products obtained from the following reaction: b. A student carried out the preceding reaction, but stopped it before it was half over, whereupon he isolated the major product. He was surprised to findthat the product he isolated was neither of the products obtained when the reaction was allowed to go to completion. What product did he isolate?
Propose a reasonable mechanism for the following reaction.
Provide the major organic product of the reaction below and a detailed, stepwise mechanis
In the below sequence of reactions, A and B are which of the following?
Give the major organic product of the following reaction sequences (d & e).
Predict and draw the major product (C11H12O2) of the following reaction sequence.
Give a clear handwritten answer..give the mechanism of given bleow reactions and label with E1,E2,SN1,SN2....
Complete the reaction by drawing the reactions major organic product and propose a detailed mecanism for it's formation
Give only typing answer with explanation and conclusion to all parts draw the mechanism for these 4 reactions with electron movement and arrows and products formed The dehydration of 2-butanol with H2SO4 The dehydration of 2-butanol with H2SO4 The dehydrobromination of 1-bromobutane with potassium tert-butoxide The dehydrobromination of 2-bromobutane with potassium tert-butoxide
the major product in the reaction sequence below is:
When the following transformation was conducted at an appropriate temperature, the following two products were formed. Provide a mechanism (all steps drawn with complete arrow pushing detail) to account for their formation. Note that n-Bu3SnH is a source of H• and is in excess