Answered: Q9. The following structure represent a…

Q9. The following structure represent a hydroxylated product of head-to-tail dimer of two isoprene units. This product is A. menthol B. camphor. C. linalool D. thymol

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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a. Draw and name all of the isomeric products obtainedfrom the monobromination of propane with Br2/light. If halogenation were a completely randomreaction and had an equal probability of occurring atany of the C—H bonds in a molecule, what percentage of each of these monobromo products would beexpected?b. Answer part (a) using 2-methylpropane as the starting material.
4G .!!: 11:09 HW-1.pdf ... Solve the following 2 Üpfaw the structure of cach of the following compounds: a. 2,3-dimethylhexane b. 4-isopropyl-2,4,5-trimethylheptane c. 4,4-diethyldecane d. 2,2-dimethyl-4-propyloctane e. 4-isobutyl-2,5-dimethyloctane f. 4-(1,1-dimethylethyl)octane Give the systematic name for each of the following compounds: CH CH3 a. CH,CH,CHCH CCH, ČH, f. CH,CH,CH,CHCH;CH,CH, CH,CHCH,CH, CH, CH,CH,CH, h. CH;CH;C(CHs)3 g. CHC- -CHCH,CH3 CH-CH;CH, c. CH;CH;C(CH;CH),CH;CH;CH3 h. CH;CH;CH,CHCHCH,CH,CH3 CHCH,) CH, d. CH CHCH;CH;CHCH, CH;CH, e. CH;CH;C(CH,CH),CH(CH)CH(CH;CH;CH)2 Give the systematic name for each of the following compounds: CH CH; e. CH;CHCHCH;CH3 CH3 b. CH CH f. CH;CH) CH:CHCH3 ČH c. HC. HC CH:CH d. h. CH,CH;CHCH3 CH CHCH
Illustrating with equations, indicate how the following substrates or reactants would be converted to their final products.
..) Fill in the blanks with the NAME and STRUCTURE of the ORGANIC REACTANT or the NAME and STRUCTURE of the MAJOR ORGANIC PRODUCT in the following reactions: Fused KOH, 200°C A. 2,2-dichloroheptane -x ? (name, str) Hydroboration В. ? --< Hexanal CH3CH2CH2CH2CH2CHO (name, str) C. ? (name, str) --Оз, НгО-- --X Butanoic acid CH3CH2CH2COOH NANH2, 150°C D. 1,2-dichlorobutane -X ?(name, str)
Draw the structure of the following three isomeric acid chlorides with chemical formula C6H₂CIO. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Consider E/Z stereochemistry of alkenes. • In cases where there is more than one answer, just give one. Acid chloride #1: cis-3-methylcyclobutanecarbonyl chloride //. | [ ]# ? ChemDoodle
Starting Materials CH3B CH3CH2BR CH3CH2CH,Br C6H5Br Reagents Mg, ether 1. a. 2. 13CH2-13C-OH b. 13CO2 then H3O* 3. LIAIH4 then H3o* PBr3 CO2 then H30* C. 4. d. 5. C6HsCH2Br е. Select a starting material and a series of reagents necessary to synthesize this compound in as few steps as possible. Enter your selection as a number for the starting material, followed by the letters of the reagents, in the order that you wish to use them, i.e. 3abcf.
Chemistry
1. Consider the structure shown on the right and answer the following questions about it (fill in blanks or circle proper choice). H 14. 1+0 140 H a. Its molecular formula is CHO and so it fits the general formula for a carbohydrate, which is C,( ). b. Specifically, this structure is (a D/ an L) (aldo/keto) (pent/hex) (ase/ose). c. Will it be optically active? d. If the top carbon was converted to a CH₂OH, would it be optically active? e. This molecule can form a six membered ring by addition of one of its -OH groups to the C-O group. Draw a circle around the -OH group which would lead to this ring. This is called a (furanose/pyranose) ring. Draw the structure of this ring in the space on the right. f. This molecule can also form a five membered ring by addition of one of its -OH groups to the C-O group. Draw a square around the -OH group which would lead to this ring. This is called a (furanose/pyranose) ring. g. In each of the rings referred to in parts e and f the carbonyl carbon…
19. e correct structure for 1-methyl-2,4,.6-trinitrobenzene(TNT) is which of the following? a. NON O2N CH3 CN- -CH3 O2N- NO2 b. d. NO2 CH3 -CH3 ON- -CH3 CH3 GON 20. The correct name for the compound given above is which of the follow ing? a. 2-cycloproproxyleyclobutane b. cyclobutylpropoxy ether с. 2-суcobutохусусlopropanе d. cyclopropoxycyclobutane 21. Of the five names listed below, four contain de liberate errors. Which is the only name is correct? a. 2-pentanal b. 2,3-dichloropentane 3-methy lpropanoic acid d. 1,2-dimethylpropanoate e. n-methy lpropanamide с.
II B. 1 for the chain propagating steps refer to the first image
Draw the structure of the molecule indicated by the IUPAC name provided. Indicate stereochemistry
keferences Draw the structure(s) of the major organic product(s) of the following reaction. H. PPH3 THE • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, draw both stereoisomers. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Include anionic counter-ions, e.g., I-, in your answer, but draw them in their own sketcher. C opy aste