Compounds X and Y both have the formula C7H14. Both X and Y react with one...
Compounds X and Y both have the formula C7H14. Both X and Y react with one molar equivalent of hydrogen in the presence of a palladium catalyst to form 2-methylhexane. The heat of hydrogenation of X is greater than that of Y. Both X and Y react with HCl to give the same single C7H15Cl compound as the major product. What are the structures of X and Y? Write all reactions, and show your reasoning.
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Compounds X and Y both have the formula C7H14. Both X and Y
react with one...
Compounds X and Y are stereoisomers having the formula C6H12. Both X and Y react with...
Compounds X and Y are stereoisomers having the formula C6H12.
Both X and Y react with one molar equivalent of hydrogen in the
presence of a palladium catalyst to form hexane, and they each
react with HBr to give a single bromoalkane product. Draw
structural formulas for both X and Y.
Compounds X and Y are stereoisomers having the formula C6H12. Both X and Y react with one molar equivalent of hydrogen in the presence of a palladium catalyst to...
[Review Topics [References] Compound X has the formula C H14 X reacts with one molar equivalent...
[Review Topics [References] Compound X has the formula C H14 X reacts with one molar equivalent of hydrogen in the presence of a palladium catalyst to form a mixture of cis- and trans-l-ethyl-3. methylcyclopentane. Treatment of X with ozone followed by zinc in aqueous acid gives a ketone and formaldehyde (CH, 0) What is the structure of X? . In cases where there is more than one answer, just draw one. -- -O0O- Compound X has the formula C,H2. X...
An alkane (A) with the formula CgH14 reacts with chlorine to yield three compounds with the...
An alkane (A) with the formula CgH14 reacts with chlorine to yield three compounds with the formula CgH13Cl: B, C, and D. Of these only C and D undergo dehydrohalogenation with sodium ethoxide in ethanol to produce an alkene. Moreover, C and D yield the same alkene E (C6H12). Hydrogenation of E produces A. Treating E with HCl produces a compound (F) that is an isomer of B, C, and D. Treating F with magnesium in dry ether followed by...
There are compounds D and compound E that react to form compound F in a one-to-one...
There are compounds D and compound E that react to form compound F in a one-to-one molar ratio. Write this reaction What would you expect the rate law to be if this reaction was elementary? The experimentally determined rate law is second order with respect to E and zeroth order with respect to D. Propose a two-step mechanism that would explain this. Identify the relative rates of each elementary step in your above mechanism (slow or fast). Draw an energy...
Two compounds, X and Y, have the formula of C7H14O. How do you determine the condensed...
Two compounds, X and Y, have the formula of C7H14O. How do you determine the condensed structural formulas and names using the following test results: compound Y forms a yellow solid in the iodoform test, but does not react with Benedict's reagent?
[Review Topics] [References) Compounds X and Y are both CH, Cl products formed in the radical...
[Review Topics] [References) Compounds X and Y are both CH, Cl products formed in the radical chlorination of 2,4-dimethylpentane. Base-promoted E2 elimination of X and Y gives, in each case, a single C H 4 alkene. Both X and Y undergo an Sy2 reaction with sodium iodide in acetone solution to give CH I products; in this reaction Y reacts faster than X What is the structure of X? . Do not use stereobonds in your answer. • In cases...
please show a detailed mechanism from X-Y, X-Z, Z-W. 2. Compound X, with chemical formula C...
please show a detailed mechanism from X-Y, X-Z, Z-W.
2. Compound X, with chemical formula C Ho, gives 1,3-dimethylcyclopentane when treated with Hz Over Pt. That same compound, when treated with hot and concentrated KMnO, produces carbon dioxide and Y. Compound X reacts with two equivalents of HBr in the presence of a peroxyether to form compound Z, with chemical formula C H2Br2. When pound Z is heated in methanol it yields compound W, among others. (a) (6 pts., 3...
Review 1opics |LKOterences Compounds X, CglH19Br, and Y, ColH19Cl, undergo base-promoted E2 elimination to give the...
Review 1opics |LKOterences Compounds X, CglH19Br, and Y, ColH19Cl, undergo base-promoted E2 elimination to give the same single alkene product, Z Catalytic hydrogenation of Z affords 2,3,3-trimethylhexane. In water X readily reacts to give a substitution product, CoH19OH, together with Z. Y does not react with water. Propose structures for X and Y. Do not use stereobonds in your answer. .In cases where there is more than one possible structure for each molecule, just give one for cach. Draw one...
Problem #1 Predict the major product(s) from the following reactions: CH3 1. 03 ? 2. DMS...
Problem #1 Predict the major product(s) from the following reactions: CH3 1. 03 ? 2. DMS b) CH₃ H₂C 1. CH2CO3H 2. H3O+ CH3 CH3 HC 1. BH3-THF 2. H2O2. NaOH CH Extra Credit An unknown compound A of molecular formula of C10H180 reacts with H2SO4 and heat to form two compounds (B and C) of molecular formula C10H16. B and C both react with H2 over Pd/C to form decalin. Ozonolysis of B forms D, and ozonolysis of C...
1.88 pts Question 2 u The structure of the anthelmintic (worm medicine) C-santonin is shown below....
1.88 pts Question 2 u The structure of the anthelmintic (worm medicine) C-santonin is shown below. What is the unsaturation number of a-santonin? CH PICH b) 5 c) 6 d) 7 o b) ) d) o e) Question 6 1.88 pts Alkenes a) have lower boiling points than alcohols of similar molar mass. b) are more dense than alcohols of similar molar mass. c) react via the sigma bond of the carbon-carbon double bond. d) both (a) and (b) e)...
Compounds X and Y are stereoisomers having the formula C6H12.
Both X and Y react with one molar equivalent of hydrogen in the
presence of a palladium catalyst to form hexane, and they each
react with HBr to give a single bromoalkane product. Draw
structural formulas for both X and Y.
Compounds X and Y are stereoisomers having the formula C6H12. Both X and Y react with one molar equivalent of hydrogen in the presence of a palladium catalyst to...
[Review Topics [References] Compound X has the formula C H14 X reacts with one molar equivalent of hydrogen in the presence of a palladium catalyst to form a mixture of cis- and trans-l-ethyl-3. methylcyclopentane. Treatment of X with ozone followed by zinc in aqueous acid gives a ketone and formaldehyde (CH, 0) What is the structure of X? . In cases where there is more than one answer, just draw one. -- -O0O- Compound X has the formula C,H2. X...
An alkane (A) with the formula CgH14 reacts with chlorine to yield three compounds with the formula CgH13Cl: B, C, and D. Of these only C and D undergo dehydrohalogenation with sodium ethoxide in ethanol to produce an alkene. Moreover, C and D yield the same alkene E (C6H12). Hydrogenation of E produces A. Treating E with HCl produces a compound (F) that is an isomer of B, C, and D. Treating F with magnesium in dry ether followed by...
There are compounds D and compound E that react to form compound F in a one-to-one molar ratio. Write this reaction What would you expect the rate law to be if this reaction was elementary? The experimentally determined rate law is second order with respect to E and zeroth order with respect to D. Propose a two-step mechanism that would explain this. Identify the relative rates of each elementary step in your above mechanism (slow or fast). Draw an energy...
[Review Topics] [References) Compounds X and Y are both CH, Cl products formed in the radical chlorination of 2,4-dimethylpentane. Base-promoted E2 elimination of X and Y gives, in each case, a single C H 4 alkene. Both X and Y undergo an Sy2 reaction with sodium iodide in acetone solution to give CH I products; in this reaction Y reacts faster than X What is the structure of X? . Do not use stereobonds in your answer. • In cases...
please show a detailed mechanism from X-Y, X-Z, Z-W.
2. Compound X, with chemical formula C Ho, gives 1,3-dimethylcyclopentane when treated with Hz Over Pt. That same compound, when treated with hot and concentrated KMnO, produces carbon dioxide and Y. Compound X reacts with two equivalents of HBr in the presence of a peroxyether to form compound Z, with chemical formula C H2Br2. When pound Z is heated in methanol it yields compound W, among others. (a) (6 pts., 3...
Review 1opics |LKOterences Compounds X, CglH19Br, and Y, ColH19Cl, undergo base-promoted E2 elimination to give the same single alkene product, Z Catalytic hydrogenation of Z affords 2,3,3-trimethylhexane. In water X readily reacts to give a substitution product, CoH19OH, together with Z. Y does not react with water. Propose structures for X and Y. Do not use stereobonds in your answer. .In cases where there is more than one possible structure for each molecule, just give one for cach. Draw one...
Problem #1 Predict the major product(s) from the following reactions: CH3 1. 03 ? 2. DMS b) CH₃ H₂C 1. CH2CO3H 2. H3O+ CH3 CH3 HC 1. BH3-THF 2. H2O2. NaOH CH Extra Credit An unknown compound A of molecular formula of C10H180 reacts with H2SO4 and heat to form two compounds (B and C) of molecular formula C10H16. B and C both react with H2 over Pd/C to form decalin. Ozonolysis of B forms D, and ozonolysis of C...
1.88 pts Question 2 u The structure of the anthelmintic (worm medicine) C-santonin is shown below. What is the unsaturation number of a-santonin? CH PICH b) 5 c) 6 d) 7 o b) ) d) o e) Question 6 1.88 pts Alkenes a) have lower boiling points than alcohols of similar molar mass. b) are more dense than alcohols of similar molar mass. c) react via the sigma bond of the carbon-carbon double bond. d) both (a) and (b) e)...
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