Compound A has the formula C10H16. When treated withhydrogen and palladium, Compound A takes up 1 equivalent ofH2, forming Compound B. When Compound A is treated withozone followed by zinc, Compound C forms with the formulaC10H16O2. Compund C is a symmetric diketone. Providestructures for Compound A and the reaction products.Select to Draw Compound BH2, Pd/C

The degree of unsaturation is C+1−(H/2) whereC = number of carbon atoms H = number of hydrogen…

Answered: Compound A has the formula C10H16. When…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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A8
Sharpless epoxidation of allylic alcohol X forms compound Y. Treatment of Y with NaOH and C6H5SH in an alcohol–water mixture forms Z. Identify the structure of Y and draw a mechanism for the conversion of Y to Z. Account for the stereochemistry of the stereogenic centers in Z. Z has been used as an intermediate in the synthesis of chiral carbohydrates.
Compound A, C₁1 H160, was found to be an optically active alcohol. Despite its apparent unsaturation, no hydrogen was absorbed on catalytic reduction over a Pd/C catalyst. On treatment of A with dilute H₂SO4, dehydration occurred and an optically inactive alkene B, C₁₁H₁4 was produced as the major product. Alkene B, on ozonolysis, gave two products. Product C, C7H6O, was shown to be an aldehyde while product D, C4H8O, was shown to be a ketone. Draw the structure of compound C. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one.
just need last answer Compound A has the formula C10H14. When treated with hydrogen and palladium, Compound A takes up 2 equivalents of H2, forming Compound B. When A is treated with ozone followed by zinc, Compound C forms with the formula C10H1404. Compund C is a symmetric structure with four identical aldehyde groups. Provide structures for Compound A and the reaction products.
I cannot figure out the structure for compound B?
Compound K, L and M are three isomers with the molecular formula C5H10O.Compound K cannot be oxidized, while compound M and L can be oxidized.Oxidation of compound L with hot acidified potassium permanganate,KMnO4 solution yields 2-methylbutanoic acid. When treated with Iodoformreagent, yellow precipitation only occurs in compound K. Fehling test onlyyielded positive results for compound L and negative for compound M andK. Compound M is then reacted with hydrogen chloride, HCl produceschlorocyclopentane (i) Draw the structural formula of compounds K, L and M.
There are three compounds with same molecular formula C8H9Br, andit has been known that all these three compounds contain a phenyl ring, anethyl group, and a bromide atom. A cannot react with AgNO3. B reactswith AgNO3 smoothly at room temperature. C can react with AgNO3 athigh temperature. Try to give the structures of A, B and C.
Isoerythrogenic acid, C18H26O2, is an acetylic 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, CH2O, malonic acid, HO2CCH2CO2H, adipic acid, HO2C(CH2)4CO2H, and the aldehyde carboxylic acid, OHC(CH2)6CO2H. Provide a structure for isoerythrogenic acid.
Benzene was reacted with chloroethane in the presence of a Lewis acid catalyst to form Compound A. Compound A was then reacted to form the compound below, labelled as B. Compound B a) Outline the mechanism for the conversion of Benzene into A. b) State the reagent & conditions required to form Compound B. Compound B was reacted with hot ethanolic potassium hydroxide to form compound C. Compound C was hydrolysed with dilute sulfuric acid to give an alcohol, compound D. c) Draw the major product formed as compound D. Finally, Compound D was reacted with benzoyl chloride to form an ester (Compound E). d) Outline the mechanism for the conversion of D into E.
Please draw out the structures of compound A, B and C. Compound A, B and C have the same molecular formula C4H6. All of the compounds can make bromine decolored. Compound A reacts with AgNO3 in ammonia solution to form white solid. Compound B undergoes cycloaddition reaction with maleic anhydride at room temperature. Compound C is oxidized with KMN04 to only give one quivalent of carboxylic acid. Please write out the structures of compound A, B and C.
Compound X (C3H6O) can be oxidised to compound Y (C3H6O2) and reduced to compound Z (C3H8O). Identify i. X ii. Y iii. Z
An optically active alkyne A (C10H14) can be catalytically hydrogenated to butylcyclohexane. Treatment of A with EtMgBr liberates no gas. Catalytic hydrogenation of A over Pd/C in the presence of quinoline poison and treatment of the product with O3 and then H2O2 gives an optically active tricarboxylic acid C8H12O6 (A tricarboxylic acids is a compound with three - CO2H groups.). Give the structure of A, and account for all observations.

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