A reaction table for the reaction of carvone with palladium on carbon* that includesreagent structures, molecular weights, intended amounts (in mmol and mg or mL),and a theoretical yield in mg and mmol. You have not been given the productstructure, but you should make a prediction based on the information given in thelab textbook and lecture. The product should be an isomer of the starting material.* for Pd/C you do not need to include a molecular weight or intended mmolPd/CPredict Product

If an excess of reagent is used, then both double bonds are reduced.

Answered: A reaction table for the reaction of…

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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What is the experimental yield of CRUDE PRODUCT AND FINAL PRODUCT (grams and percentage) Experiment: Oxidation of -Chlorotoluene to o-Chlorobenzoic acid materials used dissolved 3.35 g of KMnO4 1.20 mL of 2-chlorotoluene was added to the mixture 3.0 mL of concentrated hydrochloric acid (pH~2) 10 mL of toluene -The crystals were isolated by vacuum filtration- Product Characterization 1.15 g of the crude product 0.93 g of the final product M.p. (final): 139-141 celsius
Consider the calcination of CaCO3 Before calcination, the initial weight of CaCO3 is 1.005g. After calcination, the final weight becomes 1.0 g.Calculate the fraction reacted of CaCO3
Mass of maleic anhydride used: 5.1296 gram Volume of furan used: 3.25 ml Volume of THF used: approx. 16ml The reaction mixture was allowed to stand undisturbed for one week, whereupon, gem-like, colorless to white, prismatic crystals were isolated from the solvent matrix and allowed to air dry. When dry, the mass of the crystals was determined to be: 4.6732 gram. One small crystal was selected and ground to a fine powder for melting point measurement. The powder was observed to melt at 117 – 118 deg C. About 1ml of a saturated solution of product dissolved in DMSO-d6 was prepared and placed in an NMR tube. Subsequently, proton, carbon-13 and DEPT NMR spectra were acquired. Analysis Write the reaction using structural formulas. Calculate percent yield (show work) What does the measured melting point suggest?
On a paper, draw a schematic diagram on the Extraction of Saponins from Gugo by Lead Method using the procedures stated below. Procedures (Stas-Otto Method): Extraction of Saponins from the Gugo Bark by Lead Method Extract saponins from gugo by boiling about 10g of small pieces of gugo bark in water. (If necessary, extract first with ether or petroleum ether). Filter and add a neutral lead acetate solution to the aqueous solution; acid saponins, if present, are precipitated as lead salts. To the filtrate (including the washings, concentrated by evaporation), add basic lead acetate to precipitate neutral saponins. Wash the lead precipitate and suspend in water. Decompose by passing H2S Filter PbS and absorbed impurities. Concentrate the filtrate and finally allow to evaporate to dryness or in vacuum over H2SO4. Purify the saponins by CHCl3 and precipitate with ether. Weigh the residue and compute the percentage yield.
The aerobic oxidation of para-xylene to terephthalic acid is an important process in industrial chemistry. Discuss why the oxidation of the second methyl group requires harsher conditions than the oxidation of the first methyl group. You should accurately reference all your bibliographic material.
You are working in a plant biology laboratory that analyzes plant hormones. Your supervisor wants to use your organic chemistry knowledge to develop a protocol to separate kinetin from jasmonic acid in plant extracts. Using the same extraction conditions as for Experiment 2 (i.e. using dichloromethane and Na2CO3 aqueous solution), devise a procedure to isolate jasmonic acid. You can present your procedure in point form or as a flow chart. You can use standard reagents and techniques previously used in CHEM 266L, and state in which layer of the extraction each compound is found through your procedure.
What is main objectives in extraction of beta-carotene from carrot.
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In the synthesis of Sudan-1, the following precursors were used: Aniline – 0.2 mL β-naphthol – 0.35 g Experimental data Weight of vial, g 13.1085 Weight of vial + recrystallized product, g 13.4714 Experimental melting point, °C 129-132 Given this data: What is the theoretical yield? What is the percent yield? What is the purity of the dye based on experimental melting point (theoretical is 131-133 °C) Please show solutions and equations
One of the earliest commercial plastics was Bakelite®, formed by the reaction of phenol with a little more than one equivalent of formaldehyde under acidic or basic conditions. Baeyer first discovered this reaction in 1872, and practical methods for casting and molding Bakelite were developed around 1909. Phenol-formaldehyde plastics and resins (also called phenolics) are highly cross-linked because each phenol ring has three sites (two ortho and one para) that can be linked by condensation with formaldehyde. Suggest a general structure for a phenol-formaldehyde resin, and propose a mechanism for its formation under acidic conditions.
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