2 2. Provide the structure of the hydrocarbon that absorbs four molar equivalents of molecularhydrogen on catalytic reduction over a palladium catalyst and yields only butanedial uponozonolysis using O, followed by treatment with Zn and ACOH.3. Isoerythrogenic acid, C18H2602, is an acetylenic fatty acid that turns a vivid blue onexposure to UV light. On Catalytic hydrogenation over a palladium catalyst, five molarequivalents of hydrogen are absorbed, and stearic acid, CH3(CH2)16CO2H, is produced.Ozonolysis of isoerythrogenic acid yields the following products: formaldehyde, CH20,

Hydrocarbons are chemical compounds that consist of only carbon and hydrogen as their key elements.…

2. Provide the structure of the hydrocarbon that absorbs four molar equivalents of molecular hydrogen on catalytic reduction over a palladium catalyst and yields only butanedial upon ozonolysis using Os followed by treatment with Zn and AcOH.

2. Provide the structure of the hydrocarbon that absorbs four molar equivalents of molecular hydrogen on catalytic reduction over a palladium catalyst and yields only butanedial upon ozonolysis using Os followed by treatment with Zn and AcOH.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy

Section14.SE: Something Extra

Problem 50AP: -Ocimene is a pleasant-smelling hydrocarbon found in the leaves of certain herbs. It has the...

See similar textbooks

Related questions

Q: The product obtained when the compound below is treated with H20 under acidic condition and heating…

Q: What is the name of the mechanism where camphor is reduced to isoborneol? Is it…

A: Camphor have ketone as carbonyl group which can be reduced to OH functionality by its reduction with…

Q: Write the most stable contributing structure for the cyclohexadienyl anion formed by reaction of…

A: The most stable contributing structure is nothing but a resonating structure. In these structures,…

Q: Outline a synthesis for m-dichlorobenzene from benzene using diazonium salts as intermediates.

Q: Outline the SN2 mechanism for this reaction. for the Williamson Ether Synthesis

A: In this question we will give the SN2 mechanism of the Williamson ether synthesis of p-cresol +…

Q: In section (ii) above an acetal group is present in the starting material. Give a general reaction…

A: An acetyl is an organic compound formed by the addition of two hydroxyl group on an aldehyde or a…

Q: b) Place the styrene, TS-1, TS-2 and (R) styrene oxide and (S) styrene oxide on a single reaction…

A: In catalytic transition state, catalytic molecule combine with different transition state and…

Q: When (S)-1-bromo-1-phenylethane undergoes an SN2 reaction with methanethiol (CH3SH), the product of…

A: Answer : option (b) R only Explanation: Since in SN2 mechanism leaving Nucleophile and attacking…

Q: Compound A (C,H12) absorbed 3 equivalents of H2 on catalytic reduction over a palladium catalyst to…

Q: Compound D contains nitrogen and produces a gas upon heating with aqueous NaOH. When the resulting…

A: We have to give the structures of D, E, and F. Also, we have to give the synthesis route without the…

Q: Compound A (C9H12) absorbed 3 equivalents of H2 on catalytic reduction over a palladium catalyst to…

Q: State the effect of substituents on a benzene derivative towards further aromatic substitution

A: The effects of substituents on a benzene derivative towards further aromatic substitution:…

Q: Give the products (if any) expected from the treatment of each of the following compounds with ozone…

A: Ozonolysis:Alkene reacts with ozone which cleaves the double bond followed by work up with dimethyl…

Q: The p−toluenesulfonate shown undergoes an intramolecular Williamson reaction on treatment with base…

A: Intramolecular Williamson reaction is used to synthesize ether from organohalide and alkoxide…

Q: ) Compound AA has a molecular formula of CsHso and gives a positive result using Tollen's reagent.…

Q: Compounds X has the formula C7H15Cl; Y is C7H15Br.X undergoes base-promoted E2 elimination to give a…

A: The compound X has formula C7H15Cl.The compound Y has formula C7H15Br. It is given that catalytic…

Q: Represent the reaction mechanism of the alkene supplied to you with propanol in the presence of…

A: Alkene reacts with alcohol in presence of an acid catalyst by electrophilic addition reaction…

Q: 11. Provide the proper systematic name for the compound below. (consider and include stereochemical…

A: Rules - 1) count number of carbons in longest chain. 2) Find number of carbon that have substitution…

Q: Suggest a retrosynthesis and a synthesis for one (1) of the following compounds starting…

A: The image of the mechanism is been uploaded in step 2.

Q: Q) Write the structure of the Dieckmann cyclization product formed on treatment of each of the…

Q: [a] Provide a rationale for the fact that 3-bromobut-1-ene is the kinetically controlled product the…

Q: Using the Grignard reaction, NBS, NaCN and any other reagents, synthesize Phenylacetone from…

A: We have to prepare Phenylacetone from Toluene using grignard , NBS , NaCN and some other required…

Q: write the balanced equation and the stepwise mechanism for the Friedel-Crafts acylation of anisole…

Q: The etner ring in solamin is blosyntnesized from the diene as shown pelow. Suggest a mechanism for…

A: Due to technical error ,unable to provide you the solution. Please resubmit the question once again

Q: Provide the structure of the hydrocarbon that absorbs four molar equivalents of molecular hydrogen…

Q: . Show by means of equations the preparation of methane a. By reduction of alkyl halides b. From…

A: Preparation of methane: a. By reduction of alkyl halides b. From Grignard Reagent

Q: The Friedel-Crafts reaction of benzene with 2-chloro-3-methylbutane in the presence of AICI3 occurs…

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

Q: Define Hemiacetal, Acetal and Ketal. ii. Give the structure of the product from the reaction of…

A: Hemiacetal is a compound which is formed when alcohol reacts with aldehyde to form a product with OR…

Q: Conversion of an alkene to a halohydrin and internal displacement of a halide ion by an alkoxide ion…

Q: Give the reaction mechanism (showing curly arrows) for the bromination of methane in the presence of…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: we know that ethers, such as diethyl ether and tetrahydrofuran, are quite resistant to the action of…

A: Main difference in chemical reactivity toward dilute aqueous acid between ethers and acetals:

Q: Give all steps in the synthesis of trans- 9-(2-phenylethenyl)anthracene, starting with benzyl…

A: The following product is formed via wittig mechanism. Generally, a stable ylide can form E-alkene or…

Q: Using 1-bromobutane and any organometallic reagent among those seen in class, suggest the synthesis…

A: The details synthetic route for the reaction is provided below in attach image.

Q: Give the structure of the product and/or intermediates of the following reactions. Indicate, where…

A: Ozonolysis of alkene: One of the important reactions of alkene is ozonolysis. In the ozonolysis…

Q: Compound A has the molecular formula C14H25Br and was obtained by reaction of sodium acetylide…

A: Given, Molecular formula of compound A = C14H25Br Compound B = C14H24 Compound C = C14H26 Compound D…

Q: The hydroboration–oxidation of internal alkynes produces ketones.(a) When hydroboration–oxidation is…

A: Hydroboration-Oxidation reaction:- This reaction happens in unsaturated bonds like alkene and…

Q: A compound of cycloalkene can be prepared through dehydration of 2-methylcyclohexanol. a) Outline…

Q: (b) With correlation diagram provide the fate of (E)-1,3-pentadiene under thermal treatment.

Q: Show the electron-flow mechanism of the synthetic schemes (R-Salsolinol) of the picture below. This…

A: The detailed solution of your question given below-- Since, we know that two molecule react and…

Q: Compound C has the molecular formula C,H,, On catalytic hydrogenation, 1 mol of C absorbs 1 mol of…

A: In this question, we will Identify the starting material ( Compound C ). Given the mail Product (…

Q: Provide all resonance structures of the sigma complex when aniline reacts with an electrophile to…

A: Reaction is taking place between aniline and Br2 (Br electrophile)

Q: Write the mechanism for the nitration of toluene showing explicitly why ortho and para products are…

A: We have to show mechanism for nitration of toluene showing why ortho and para product favoured over…

Q: Give the reaction mechanism (showing curly arrows) for the bromination of methane in the presence of…

A: Here we are required to show the mechanism of the reaction

Q: Give the structure of the product from the reaction of propanal with 1M ethanol in dry acid.…

A: In the reaction between aldehyde and alcohol in presence of acid, hemiacetal is produced.

Concept explainers

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.

Question

2. Provide the structure of the hydrocarbon that absorbs four molar equivalents of molecular
hydrogen on catalytic reduction over a palladium catalyst and yields only butanedial upon
ozonolysis using O, followed by treatment with Zn and ACOH.
3. Isoerythrogenic acid, C18H2602, is an acetylenic fatty acid that turns a vivid blue on
exposure to UV light. On Catalytic hydrogenation over a palladium catalyst, five molar
equivalents of hydrogen are absorbed, and stearic acid, CH3(CH2)16CO2H, is produced.
Ozonolysis of isoerythrogenic acid yields the following products: formaldehyde, CH20,

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-Introduction

VIEW

Step 2-Identification of the hydrocarbon

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 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

Two isomers, A and B, of molecular formula C5H8 undergo catalytic hydrogenation with hydrogen gas and palladium on carbon to form the same C5H10 product. On ozonolysis followed by treatment with hydrogen peroxide (H2O2), isomer A gave a product of molecular formula C5H8O4 that has two carboxylic acid groups in it whereas isomer B gave a product of molecular formula C5H8O3 that contains a carboxylic acid group and a ketone group. Which of the following isomeric pairs best match this data?
Two isomers, A and B, of molecular formula C5H8 undergo catalytic hydrogenation with hydrogen gas and palladium on carbon to form the same C5H10 product. On ozonolysis followed by treatment with hydrogen peroxide (H2O2), isomer A gave a product of molecular formula C5H8O4 that has two carboxylic acid groups in it whereas isomer B gave a product of molecular formula C5H8O3 that contains a carboxylic acid group and a ketone group. What is the isometric pair of A and B that corresponds?
A terminal alkyne was treated with NaNH2 followed by 1-iodopropane. The resulting internal alkyne was treated with ozone followed by water, giving only one type of carboxylic acid. Provide a systematic, IUPAC name for the internal alkyne.
Compound A (C9H12) absorbed 3 equivalents of H2 on catalytic reduction over a palladium catalyst to give B(C9H18). On ozonolysis, compound A gave, among other things, a ketone that was identified as cyclohexanone. Ontreatment with NaNH2 in NH3, followed by addition of iodomethane, compound A gave a new hydrocarbon, C(C10H14 ) . What are the structures of A, B, a nd C?
A hydrocarbon (X), with the molecular formula: C8H14 is reduced in presence of sodium and liquid ammonia to give the only product (Y) with the molecular formula: C8H16. Compounds X and Y both resulting 2,5-dimethylhexane when treated with hydrogen and platinum catalyst (H2/Pt). As a result of the oxidative cleavage of compound Y (by using KMnO4 / H2SO4), a single carboxylic acid derivative with C4H8O2 molecular formula is formed. Again, as a result of the reaction of Y with perbenzoic acid, the chiral compound C8H14O is observed, but the reaction of compound Y with bromine gives the achiral C8H14Br2 as the product.
(a) Illustrate the following name reactions by giving example :(i) Cannizzaro’s reaction(ii) Clemmensen reduction(b) An organic compound A contains 69.77% carbon, 11.63% hydrogen and rest oxygen. The molecular mass of the compound is 86. It does not reduce Tollen’s reagent but forms an addition compound with sodium hydrogen sulphite and gives positive iodoform test. On vigorous oxidation it gives ethanoic and propanoic acids. Derive the possible structure of compound A.
Ozonolysis of compound D will produce compound E and compound F as products. Hydrationof compound D will produce compound G as major product. Compound D is a major productobtained from dehydrohalogenation of 2-chloro-3-methylbutane. a) Identify the structural formula for compound D, E, F and G.b) Suggest suitable reagent(s) and condition(s) needed for dehydrohalogenation of 2-chloro-3-methylbutane
1. Compound A, C9H12, absorbs 3 equivalents of H2 on catalytic hydrogenation over palladium catalyst to give B, C9H18. On the treatment with acidic KMnO4, compound A gives among other things, a ketone that was identified as cyclohexanone. On reaction with NaNH2 in NH3, followed by addition of iodomethane, compound A gives a new hydrocarbon C, C10H14. What are the structures of A , B and C?
Define Hemiacetal, Acetal and Ketal. Give the structure of the product from the reaction of propanal with 1M ethanolin dry acid. What happens when Further 1M of ethanol is added to above?
Compounds X has the formula C7H15Cl; Y is C7H15Br.X undergoes base-promoted E2 elimination to give a single alkene product Z. Y likewise reacts under similar conditions to give a single alkene product that is isomeric with ZCatalytic hydrogenation of Z affords 3-ethylpentane.X readily reacts in SN2 fashion with sodium iodide in acetone. Y does not undergo a similar SN2 reaction. Propose structures for X and Y.
Stearolic acid, C18H32O2, yields stearic acid on catalytic hydrogenation and undergoes oxidative cleavage with ozone to yield nonanoic acid and nonanedioic acid. What is the structure of stearolic acid?
1.Describe the ozonolysis of alkenes 2.one mole of a hydrocarbon(A) reacts with one mole of beomine giving a dibromo compound C5H10Br2.Substance A on treatment with cold dilute kMnO4 solution forms a compound C5C12O2(C5H12O2) on ozonolysis A,gives equimolar quantities of propanone and ethanol.Deduce the structure of substance A.