Predict the Product. Provide the stable organic product(s) for the reactions below.1.MgBr(1 eq.), THF2. HCI, НаО3. O1. Mg, diethyl etherBr2. CH,OD

Here, the both reactions are grignard reactions. The mechanism is shown below -

Answered: Predict the Product. Provide the stable…

Predict the Product. Provide the stable organic product(s) for the reactions below. „MgBr (1 eq.), THE 2. HCI, H,0 3. 1. Mg*, diethyl ether Br 2. CH,OD

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter7: Alkynes

Section: Chapter Questions

Problem 7.35P

See similar textbooks

Related questions

Q: A synthesis of 2-butanol was performed by treating 2-bromobutane with hot sodium hydroxide solution.…

Q: 3. Illustrate all the possible reaction for toluene.

A: Toluene contain methyl group in benzene ring and it is electrons donating group because CH3 donate…

Q: Br The alcohol compound given the formula below is used in perfume making. Demonstrate the synthesis…

Q: Part 5: Predict the products of the dehydration reaction below AND name them. он н н н-с—с—с—с—с-н…

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

Q: The Gabriel synthesis is a two-step preparation for primary amines, with the alkylation of potassium…

Q: How is electron-withdrawing resonance effects on substitution reaction of benzene? Explain the…

A: Electron withdrawing groups(EWG) are the groups which pulls the electron density from the system(to…

Q: 1) For parts a and b, provide structures for alkenes that would give the indicated reaction…

A: Q-1-a Hydroboration–oxidation reaction is a two step reaction to form alcohol from the alkene.

Q: 3. Assuming we start with 200 mg of cyclopentadiene and 300 mg of maleic anhydride, and 375 mg of…

A: The reaction of cyclopentadiene with maleic anhydride giving cycloadduct anhydride can be given as:…

Q: Write equations for the reaction of 2-butanol with reagent. Where you predict no reaction, write…

A: The conditions of the strong oxidizing agents along with the acidic environment oxidize the…

Q: The same alkane is obtained from the catalytic hydrogenation of both alkene A and alkene B. The heat…

A: The same alkane is obtained from the catalytic hydrogenation of both alkene A and alkene B. The heat…

Q: An unknown alcohol C6H14O gave a rapid Lucas Test. It could not be oxidized easily, but upon…

A: DBE of the alcohol = (C+1)-H/2 = (6+1)-14/2 = 0. Hence, it is an aliphatic alcohol. According to…

Q: Write the structural formula and name of the organic product for the reaction between an alkyne and…

Q: 5. An unknown hydrocarbon A with the formula C6H12 reacts with 1 molar equivalent of H2 over a…

A: The given unknown hydrocarbon A with formula C6H12reacts with 1 molar equivalent of H2 over a Pd…

Q: 3. Write the structure of the alkene X, that forms the compound below, when treated with ozone (03)…

A: The following reaction is referred as the oxidative cleavage of alkene.

Q: A compound of structural formula, NH,CH2CO,H can be obtained: 38. from the hydrolysis of…

A: (1) When ethanenitrile is hydrolyzed then imidic acid is formed as - CH3-CN + OH- ---->…

Q: Compound A has the formula C8H8. It reacts rapidly with KMNO4 to give CO2 and a carboxylic acid, B…

Q: - The compound (X) is formed from catalytic hydration of ethene. The compound (X) react with the…

Q: The difference in melting points between trans-oleic acid (18:1,D9)(44.5C) and cis-oleic acid…

A: given data is trans-oleic acid (18:1,D9) melting point is (44.50C) cis-oleic acid melting point is…

Q: In the reaction of 3-hexene with HBr, which of the products is expected to be formed in a larger…

A: Alkenes are the compounds which contain one or more double bonds. The starting material is 3-hexene.…

Q: HBr Br Iv, heat Cl2 H,0

Q: Draw the organic products of the reaction shown. Draw hydrogens on oxygen and nitrogen where…

Q: Give the major organic product(s) of the following reaction. CrO3 ? OH H2S04

Q: A hydrocarbon with IHD of 2 showed persisting yellow color in the bromine test. What is the likely…

A: Identity of compound on the basis of Bromine test.

Q: (1) For the following S-containing organic compounds, draw its structures and give its IUPAC and…

Q: Write equations for the reaction of 1-butanol with reagent. Where you predict no reaction, write…

A: The reaction is as given below:

Q: Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the…

Q: An organic chemist reacts 1-butanol with SOCI2 in pyridine, removes the major organic product, and…

A: SOCl2 converts alcohol to chloroakane . In the second step, CN- group substitute Cl atom from…

Q: Theoretical mass of P-Coumaric acid is 164.16, in LCMS analysis it observed 146.9 why this is so?…

A: The observed mass of P-Coumaric acid mentioned in the question is actually its mass-to-charge ratio…

Q: Question 17 Provide the structure(s) of the expected major organic product from the following…

A: The reaction competition is given below with the major organic product formed:

Q: write the product of the D-gulose reaction by: a. CH3I, Ag2O b. The product in (a), then H3O+ c.…

A: Number of functional group is associated with organic compounds which impart specific chemical and…

Q: After performing all of the necessary calculations, the appropriate glassware and reaction…

A: The hydrolysis reaction taking place is given as,

Q: question 1 i) Explain the acidity of terminal alkanes, alkenes and alkynes. ii) Compound A has the…

A: Double bond equivalence (DBE) for the molecular formula C10H16 can be calculated by using the…

Q: H2O2. + HCI H2O2 + HBr 1. ВН3, THF 2. НО, Н-О2, Н20

Q: An unknown hydrocarbon A with the formula C6H12 reacts with 1 molar equivalent of H2 over a…

A: Reduction of alkene gives alkane.

Q: Which of the following statements about 3-iodo-2-methylprop-1-ene is/are true? (i) It has an E…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. NH₂ NaNO₂ aqueous…

A: Note : P-cyano aniline reacts with NaNO2 and HCl produces p-cyanobenzene diazonium chloride. ( see…

Q: H,0, H,SO, НОСН CI D2, Pt SOCI, Pyridine HO. Br

Q: (B). Write the chemical reactions of 2-chloro-2-methylbutane with the following two sets of…

Q: Industrial Chemistry 2.1. Why are so many routes available for the creation of acetic acid? 2.2.…

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

Q: 1. The line structure of a natural product that was isolated from various shrubs is shown below.…

A: Hi there! Thank you for the question, but as per our guidelines, we can solve only one question at a…

Q: a) How can TLC allow you to determine if your reaction takes place. Explain. b) How can TLC allow…

A: TLC stands for Thin Layer Chromatography. It is basically an identification and separation technique…

Q: Write the structural formula and name of the organic product for the reaction between an alkyne and…

A: Alkyne contains acidic hydrogen and in presence of a base (NaNH2), the acidic hydrogen is removed to…

Q: Give the major product(s) of the following reaction. CH3CH2CH=CH2 (1 mole) HCI, AICI3, heat

Concept explainers

UV Visible Spectroscopy

Spectroscopy refers to the absorption or emission of light or other radiations by matter. When a substance or chemical absorbs light or radiation, they reach an excited state followed by de-excitation or emission of the light or radiation forming distinct spectra. UV-visible spectroscopy or ultraviolet-visible refers to the absorption and emission in the ultraviolet and visible regions of the electromagnetic spectrum.

Question

100%

Predict the Product. Provide the stable organic product(s) for the reactions below.
1.
MgBr
(1 eq.), THF
2. HCI, НаО
3. O
1. Mg, diethyl ether
Br
2. CH,OD

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 2 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

1. In the reactions involving the three isomeric alcohols with the formula C4H9OH, describewhat each of the following tests showed about reactivity of the -OH group and reactions of 1°,2°, and 3° alcohols.• the test with neutral KMnO4• the test with concentrated HCl2. Predict how the fourth alcohol with the formula C4H10O would react if tested with:• 0.01 M KMnO4• concentrated HCl at room temperatureExtend FurtherUse your observations of the solutions formed in the previous experiments and yourunderstanding of alcohols to complete a table like the one shown below. Research the meltingand boiling points to verify your answers.
Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the presence of H2SO4 and provide a clear rationale as to why this is the major product of the reaction and the minor product of the reaction.
1. what are the differences between acyclic and cyclic forms in terms of their physical properties? 2. what is the role of vinegar in liquid-liquid extraction?
COMPLETE THE TWO REACTIONS BELOW
Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the presence of H2SO4 and provide a clear rationale as to why this is the major product of the reaction.
i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,
C6H5CO2CH2C6H5 can be synthesized by an SN2 reaction. Draw the structures of the alkyl chloride and nucleophile that will give this compound in highest yield. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include all valence lone pairs in your answer. Separate multiple reactants using the + sign from the drop-down menu. When a metal counterion is needed, use Na+, but draw it in its own sketcher.
Disiamylborane adds only once to alkynes by virtue of its two bulky secondary isoamylgroups. Disiamylborane is prepared by the reaction of BH3 # THF with an alkene.(a) Draw the structural formulas of the reagents and the products in the preparation ofdisiamylborane.(b) Explain why the reaction in part (a) goes only as far as the dialkylborane. Why isSia3B not formed?
Following compounds are given to you:2-Bromopentane, 2-Bromo-2-methylbutane, 1-Bromopentane(i) Write the compound which is most reactive towards SN2 reaction.(ii) Write the compound which is optically active.(iii) Write the compound which is most reactive towards β – elimination reaction
You are required to synthesize 2-bromopentane from the reaction between an alkene with HBr. Which alkene, 1-pentene or 2-pentene, should you react with HBr in order to get 2-bromopentane? Give an explanation.
The standard procedure for synthesizing a compound is the stepwise progress toward a target molecule by forming individual bonds through single reactions. Typically, the product of each reaction is isolated and purified before the next reaction in the sequence is carried out. One of the ways nature avoids this tedious practice of isolation and purification is by the use of a domino sequence in which each new product is built on a preexisting one in stepwise fashion. A great example of a laboratory domino reaction is William S. Johnsons elegant synthesis of the female hormone progesterone. Johnson first constructed the polyunsaturated monocyclic 3 alcohol (A) and then, in an acid-induced domino reaction, formed compound B, which he then converted to progesterone. A remarkable feature of this synthesis is that compound A, which has only one stereo-center, gives compound B, which has five stereocenters, each with the same configuration as those in progesterone. We will return to the chemistry of Step 2 in Section 16.7 and to the chemistry of Steps 3 and 4 in Chapter 19. In this problem, we focus on Step 1. (a) Assume that the domino reaction in Step 1 is initiated by protonation of the 3 alcohol in compound A followed by loss of H2O to give a 3 carbocation. Show how the series of reactions initiated by the formation of this cation gives compound B. (b) If you have access to a large enough set of molecular models or to a computer modeling program, build a model of progesterone and describe the conformation of each ring. There are two methyl groups and three hydrogen atoms at the set of ring junctions in progesterone. Which of these five groups occupies an equatorial position? Which occupies an axial position?
Chlorination of 2-butanone yields two isomeric products, each having the molecular formula C4H7ClO. (a) What are these two compounds? (b) Write structural formulas for the enol intermediates that lead to each of these compounds. (c) Using curved arrows, show the flow of electrons in the reaction of each of the enols with Cl2.