Answered: What is the major organic product…

What is the major organic product formed, when 3-methylbut-1-ene undergoes hydrohalogenation in presence of HBr? (A) (В) Br Br Br (C) (D) Br

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 53AP

See similar textbooks

Related questions

Q: Which of the attached compounds undergo Friedel–Crafts alkylation with CH3Cl and AlCl3? Draw the…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Oxidation of cholesterol converts the alcohol to a ketone. Under acidic or basic…

A: The structure of cholesterol and cholest-4-ene-3-one are given below.

Q: Cyclohexene is treated with cold diluted KMnO4. The spatial arrangement of the two hydroxy groups in…

Q: What alkynes give each of the following ketones as the only product after hydration with H2O, H2SO4,…

Q: Which of the following set of reagents will yield a vicinal diol when reacted with an alkene? a…

A: ->Vicinal diol is Compound in which -OH group attached at adjacent carbons.

Q: Cyclopentene reacts with reacts with ozone in dichloromethane at -78° C. Treatment of the resulting…

Q: Jiadifenin is a natural product isolated from the fruit of the Chinese plant Illicium jiadifengpi,…

A: A stepwise mechanism for the conversion of M to N has to be drawn.

Q: 6. Provide the line structure of product E in the following reaction. Include stereochemistry for…

Q: "Use the three reaction conditions for hydration of an alkene to convert A-C or D-F to alcohols, and…

A: This is the question of reaction mechanism.In this reaction Alkene is react with appropriate reagent…

Q: 5) 2-methyl-1,3-cyclohexadiene is treated with 1 equivalent of HCl. There are two major products.…

A: Applying concept of 1,2 and 1,4 addition reaction at conjugated diene.

Q: Decane undergoes thermal cracking to produce compound D and compound E with equal number of carbon…

A: Thermal cracking is the process where hydrocarbons are subjected to high temperature and pressure to…

Q: Which of the following alkenes will yield a meso dihalide when reacted with Br/CCh at room…

A: Alkene reacts with bromine to form dibromoalkane. The reaction proceeds by the bromonium ion…

Q: (a) Compound D undergoes a reaction with hydrogen bromide, HBr to produce 2-bromobutane. D exists as…

A: Alkenes and alkynes can decolourises bromine solution in methylene chloride. Colour changes from a…

Q: Several steps in the synthesis of optically active duloxetine, an antidepressant sold under the…

A: Intermediate A is produced by asymmetric reduction of 3-chloro-1-(thiophen-2-yl)propan-1-one by (R)-…

Q: The hemiacetal product of the following reaction is он OH он он он 333333

A: In the above reaction, since the ketone is having a carbon with partial +ve charge (the one which is…

Q: to Br B A

Q: Q3. 2-Bromopentane, when treated with alcoholic KOH yields a mixture of three alkenes A, B andC.…

A: E2 elimination is a type of elimination reaction in which the removal of a proton by a base and the…

Q: Phenylacetaldehyde is partly responsible for the fragrance of the flowers of the plumeria tree,…

A: The carbonyl compounds give nucleophilic addition reactions. The carbon atom of the carbonyl carbon…

Q: When attached halohydrin is treated with NaH, a product of molecular formula C4H8O is formed. Draw…

A: In the given reaction, halohydrin is treated with NaH. When a halohydrin is treated with a base…

Q: When attached halohydrin is treated with NaH, a product of molecularformula C4H8O is formed. Draw…

A: In the given reaction, halohydrin is treated with sodium hydride (NaH). When a halohydrin is treated…

Q: Which of the compounds A-D are obtained in the reaction of the alkene below with OsO4 in pyridine…

A: Osmium tetroxide reacts with alkene to produce cis di-ol.

Q: 4.22 Name the following alkynes, and predict the products of their reaction with (i) H2 in the…

A: A question based on alkynes that is to be accomplished.

Q: Draw the product formed when the following compound undergoes an electrocyclic reaction a. under…

A: a. Under thermal conditions, it follows conrotatory mode of cyclisation and gives cis configuration

Q: When alkyne A is treated with NaNH2 followed by CH3I, a product havingmolecular formula C6H10O is…

A: In 4-pentyn-1-ol, the O-H bond is more acidic than acetylenic C-H bond. The base abstracts the H…

Q: (a) Why does p-dichlorobenzene have a higher m.p. than its o- and m-isomers?(b) Why is…

A: (a) The structure of p-dichlorobenzene and its o- and m-isomers are as follows: As you can…

Q: When alkyne A is treated with NaNH2 followed by CH3I, a product having molecular formula C6H10O is…

A: The hydrogen attached with sp hybridized carbon is highly acidic because it contains the electron in…

Q: Q3\ The pKa of p-cyclopropylbenzoic acid is 4.45. Is cyclopropylbenzene likely to be more reactive…

Q: 6. What is the relationship between A and B? HO OH II A) They are constitutional isomers They are…

Q: Suzuki coupling of aryl iodide A and vinylborane B affords compound C, which is converted to D in…

A: The compound C formed in the reaction is shown below.

Q: Compound Y has molecular formula C7H12. Hydrogenation of compound Y produces methylcyclohexane.…

A: Compound Y has molecule formula, C7H12

Q: Which of the possible stereoisomers are formed by oxidation of (S )-4-methylcyclohexene with osmium…

A: Alkene (A) undergoes oxidation using osmium tetra oxide gives cyclic osmate intermediate, this…

Q: The sex attractant given off by the common house fly is a simple alkene named muscalure,{CH3…

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: 3. (a) Identify the reagents (A-D) in each of the following reactions. OTS OH B он HOCI OH…

A: Since you have asked a question with multiple sub-parts, we will solve first three sub-parts for…

Q: 1. Write out all the isomers of the compound with molecular formula C,H19O a. Select the normal/…

Q: What is the structure of cis-jasmone, a natural product isolated from jasmine flowers, formed by…

A: Since the treatment of any alkyne with H2 in the presence of the Lindlar catalyst reduces the…

Q: 3. What alkene with the molecular formula C6H12, when treated with ozone and then dimethyl sulfide,…

A: The reaction of an alkene or alkyne molecule in the presence of ozone O3 and reducing agent is…

Q: Q3. 2-Bromopentane, when treated with alcoholic KOH yields a mixture of three alkenes A, B and C.…

A: Dehydrohalogenation involves the removal of the halogen atom together with a hydrogen atom from a…

Q: What is the structure of cis-jasmone, a natural product isolated from jasmine flowers, formed by…

A: What is the structure of cis-jasmone, a natural product isolated from jasmine flowers, formed by…

Q: b. с. a. NH2 d. e. O-CH,

Q: Cyclohexene (an alkene) is mixed with potassium permanagnate solution (KMnO4). What do you expect to…

A: KMnO4 is a strong oxidising agent, it itself got reduced and oxidise the reactant present i.e.…

Q: Account for the regioselectivity and stereoselectivity observed when 1-methylcyclopentene is treated…

A: Stereoselectivity comes in the first step when Hg(OAc)2 react with an alkene. In…

Q: (S)-2-butanol reacts with potassium dichromate (K2CIO4) in aqueous sulfuric acid to give A(C,HgO).…

A: Secondary alcohol oxidized into ketone and ketone given nucleophilic addition reaction with the…

Q: Which of the following reagents could be used to effect the transformation shown to give the…

A: Base abstracts a proton to give alkene.

Q: Suzuki coupling of aryl iodide A and vinylborane B affords compound C, which is converted to D in…

A: The compound C formed in the reaction is shown below.

Q: Identify the product formed when benzene is treated with the acyl chloride shown below in the…

A: The given reaction is Fridel-craft Acylation reaction. We know that Fridel-crafts Acylation…

Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

What is the major organic product formed, when 3-methylbut-1-ene undergoes
hydrohalogenation in presence of HBr?
(A)
(В)
Br
Br
Br
(C)
(D)
Br

Expert Solution

This question has been solved!

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

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step 3

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

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

Draw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by hydrolysis with NaHSO3 + H2O. Explain how these reactions illustrate that syn dihydroxylation is stereospecific.
Draw the products formed when both cis- and trans-but-2-ene are treated with a peroxyacid followed by -OH (in H2O).Explain how these reactions illustrate that anti dihydroxylation is stereospecic.
Draw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by hydrolysis with NaHSO3 + H2O. Explain how these reactions illustrate that syn dihydroxylation is stereospecic.
Draw the organic products formed when cyclopentene is treated withfollowing reagent. (CH3)3COOH, Ti[OCH(CH3)2]4, (−)-DET
2,3-Dimethylfumaric acid has a molecular formula C6H8O4. It undergoes oxidativecleavage to form two identical compound N. Compound N is then reacted withethylmagnesium bromide to form compound O. Compound O is then hydrolysed inacidic condition to form compound P. Draw the structure of compound N, O and P. PLEASE PROVIDE CLEAR HANDWRITING, and explantion
Name the structure. Heating compound A in the presence of H2SO4 results in which product?
Which of the following alkene reactions occurs with a complete cleavage of the C=C ( breaking both pi and sigma bond components) ? Select one: A. Alkene + H2O2 with catalytic amount of OsO4 B. Reaction of an alkene with KMnO4/OH- at room temperature. C. Treating the alkene with O3 gas, followed by reduction with Zn / H2O D. Reaction of an alkene with water (H2O) in the presence of a H+ catalyst.
What stereoisomers are formed when pent-1-ene is treated with H2O and H2SO4?
Friedel–Crafts alkylation of benzene with (R)-2-chlorobutane and AlCl3 affords sec-butylbenzene.a. How many stereogenic centers are present in the product?b. Would you expect the product to exhibit optical activity? Explain, with reference to the mechanism.
What is the major product formed when 3-methyl-1-butene is treated with Hg(C2H3O2)2 in a THF/ethanol mixture followed by NaBH4 in base?
Deduce the structure of each compound from the information given. All unknowns in this problem have molecularformula C8H12.(a) Upon catalytic hydrogenation, unknown W gives cyclooctane. Ozonolysis of W, followed by reduction with dimethylsulfide, gives octanedioic acid, HOOC¬(CH2)6¬COOH. Draw the structure of W
Write out all the isomers of the compound with molecular formula C4H10O . Select the normal/ primaryisomer and treat it with conc. H2SO4 and heat. Identify the reaction and give the product ‘A’ from it. 2. When ‘A’ is treated with HBr in the presence of a peroxide, give the name and structure of the product.