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Compound, C, has the molecular formula C7H 12. On catalytic hydrogenation, 1 mol of C absorbs...
5. The sex attractant by which the female housefly attracts the male has the molecular formula...
5. The sex attractant by which the female housefly attracts the male has the molecular formula C23H4s Catalytic hydrogenation yields an alkane of molecular formula C23H48. Ozonolysis yields CH3(CH2)-CH and CH(CH2)12CH What is the structure of the housefly sex attractant?
please explain 4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar...
please explain
4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in the unknown compound? b) How many triple bonds are present? c) How many double bonds are present? d) How many rings are present? e) Draw a structure that fits the data
4. An unknown hydrocarbon has...
Answer all Answer all 4. What is the structure of the compound that gives the IR...
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4. What is the structure of the compound that gives the IR and proton NMR spectra? Examine the H NMR of each structure as a review. Note the chemical shift for each proton 100 MHz proton NMR spectrum CDC13 solution 2270 IR Spectrum (liquid film) 1745 - 4000 3000 1200 800 TMS 2000 1600 fem') oppm) O HƏNCH:C=c-c-OCH; NEC-CH:-0-OCH:CH; o 1,6--OCH HC --CHÚC H:C-C-OCH:CH.CN H;CCH: -2-0-CH:CN 1. Compound, B, has the molecular formula C7H12. On catalytic...
11. (6 pts) Hydrocarbon A has the formula C8H10. Compound A absorbs three equivalents of H2...
11. (6 pts) Hydrocarbon A has the formula C8H10. Compound A absorbs three equivalents of H2 are upon catalytic hydrogenation. When Compound A is treated with KMnO4 the following compounds form. What is the structure of A? O C-OH + HO-C-CH,CHCH2-C-OH CH3 -C-OH 3° unsat 3 the equiv
Insert Delete F12 CHM210 Homework #7 Fall 2019 4. Compound A has the molecular formula C&H14....
Insert Delete F12 CHM210 Homework #7 Fall 2019 4. Compound A has the molecular formula C&H14. Upon catalytic hydrogenation over Pa/C it reacts with only one equivalent of hydrogen. Suggest a possible structure for Compound A. (There are MANY possible correct answers here.) Praw all of the dehydration products that are formed from the following compound.
An optically active compound A with molecular formula C8H14 undergoes catalytic hydrogenation to give an optically inac...
An optically active compound A with molecular formula C8H14
undergoes catalytic hydrogenation to give an optically inactive
product. Which of the following structures for A is (are)
consistent with all the data?
Practice Problem 09.47 Compound A has the molecular formula Cy112. Hydrogenation of compound A produces 2-methylhexane,...
Practice Problem 09.47 Compound A has the molecular formula Cy112. Hydrogenation of compound A produces 2-methylhexane, Hydroboration-oxidation of compound A produces an aldehyde. Get help answering Molecular Drawing Correct. Draw the structure of compound A. Get help answering Molecular Drawing que Incorrect x Incorrect. Draw the structure of the aldehyde produced upon hydroboration-oxidation of compound A. H2C Mawa Edit CH₃
1. A compound has molecular formula of C8H8O and every mole of this compound is able...
1. A compound has molecular formula of C8H8O and every mole of this compound is able to react with 4 moles of H2 in a complete catalytic hydrogenation. How many ring(s) is/are there in this compound? ___ How many pi bond(s) is/are there in this compound? ____ 2. A compound has molecular formula of C6H8O and every mole of this compound is able to react with 1 mole of H2 in a complete catalytic hydrogenation. How many ring(s) is/are there...
Deduce the structure of each compound from the information given. All unknowns in this problem have...
Deduce the structure of each compound from the information given. All unknowns in this problem have molecular formula C8H12.(a) Upon catalytic hydrogenation, unknown W gives cyclooctane. Ozonolysis of W, followed by reduction with dimethyl sulfide, gives octanedioic acid, HOOC — (CH2)6 — COOH. Draw the structure of W.(b) Upon catalytic hydrogenation, unknown X gives cyclooctane. Ozonolysis of X, followed by reduction with dimethyl sulfide, gives two equivalents of butanedial, O=CH — CH2CH2—CH = O. Draw the structure of X.(c) Upon...
An unknown compound A has the molecular formula C7H1402. Compound A absorbs strongly in the IR...
An unknown compound A has the molecular formula C7H1402. Compound A absorbs strongly in the IR at 1700 cm! The 'H NMR spectral data for compound A are given below. What is the structure of compound A? absorption ppm ratio of absorbing H'S singlet 10 triplet 1.2 quartet 35
5. The sex attractant by which the female housefly attracts the male has the molecular formula C23H4s Catalytic hydrogenation yields an alkane of molecular formula C23H48. Ozonolysis yields CH3(CH2)-CH and CH(CH2)12CH What is the structure of the housefly sex attractant?
please explain
4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in the unknown compound? b) How many triple bonds are present? c) How many double bonds are present? d) How many rings are present? e) Draw a structure that fits the data
4. An unknown hydrocarbon has...
Answer all
Answer all
4. What is the structure of the compound that gives the IR and proton NMR spectra? Examine the H NMR of each structure as a review. Note the chemical shift for each proton 100 MHz proton NMR spectrum CDC13 solution 2270 IR Spectrum (liquid film) 1745 - 4000 3000 1200 800 TMS 2000 1600 fem') oppm) O HƏNCH:C=c-c-OCH; NEC-CH:-0-OCH:CH; o 1,6--OCH HC --CHÚC H:C-C-OCH:CH.CN H;CCH: -2-0-CH:CN 1. Compound, B, has the molecular formula C7H12. On catalytic...
11. (6 pts) Hydrocarbon A has the formula C8H10. Compound A absorbs three equivalents of H2 are upon catalytic hydrogenation. When Compound A is treated with KMnO4 the following compounds form. What is the structure of A? O C-OH + HO-C-CH,CHCH2-C-OH CH3 -C-OH 3° unsat 3 the equiv
Insert Delete F12 CHM210 Homework #7 Fall 2019 4. Compound A has the molecular formula C&H14. Upon catalytic hydrogenation over Pa/C it reacts with only one equivalent of hydrogen. Suggest a possible structure for Compound A. (There are MANY possible correct answers here.) Praw all of the dehydration products that are formed from the following compound.
An optically active compound A with molecular formula C8H14
undergoes catalytic hydrogenation to give an optically inactive
product. Which of the following structures for A is (are)
consistent with all the data?
Practice Problem 09.47 Compound A has the molecular formula Cy112. Hydrogenation of compound A produces 2-methylhexane, Hydroboration-oxidation of compound A produces an aldehyde. Get help answering Molecular Drawing Correct. Draw the structure of compound A. Get help answering Molecular Drawing que Incorrect x Incorrect. Draw the structure of the aldehyde produced upon hydroboration-oxidation of compound A. H2C Mawa Edit CH₃
An unknown compound A has the molecular formula C7H1402. Compound A absorbs strongly in the IR at 1700 cm! The 'H NMR spectral data for compound A are given below. What is the structure of compound A? absorption ppm ratio of absorbing H'S singlet 10 triplet 1.2 quartet 35
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