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You have an unknown molecule, Molecule Q, which has a molecular formula of C_10H_18. When you...
4. Molecule W has the molecular formula C&H. When Molecule W is reacted first with BH3...
4. Molecule W has the molecular formula C&H. When Molecule W is reacted first with BH3 in tetrahydrofuran (THF) then treated with basic hydrogen peroxide the resulting products are an optically inactive mixture of molecules H and A. When molecule Wis treated with warm KMnO4 followed by an acidic water treatment the molecule below is the product. Draw out the structure for molecules W. H and A? You must show all of your work in order to earn full credit...
. When Molecule W is reacted first with cules H and A. When molecule Wis 4....
. When Molecule W is reacted first with cules H and A. When molecule Wis 4. Molecule W has the molecular formula C8H14. When Molecule W is reaca BH3 in tetrahydrofuran (THF) then treated with basic hydrogen peroxide the resu eroxide the resulting products are an optically inactive mixture of molecules H and A. When more treated with warm KMnO4 followed by an acidic water treatment the molecule the product. Draw out the structure for molecules W, H and A?...
6. An organic compound U with molecular formula C19H38 gave 2, 6, 12, 14- tetramethylpentadecane on...
6. An organic compound U with molecular formula C19H38 gave 2, 6, 12, 14- tetramethylpentadecane on hydrogenation. Ozonolysis of U gave propanone and a 16- carbon aldehyde V as products. Give the structures of U and V and provide the name for U. 7. An unknown hydrocarbon Q has a formula CaH12. Q Reacts with osmium tetroxide to give a diol R. When oxidized with KM O4 in an acidic medium, Q gives two products. One product is propanoic acid...
i'm having trouble going backwards in reactions. if you have any tips please share. thank you!...
i'm having trouble going backwards in reactions. if you have
any tips please share. thank you!
3. For each reaction determine the reactant that lead to the formation of the indicated products. (3 points each) 3a. 1. KMnO4, warm 2. H, H20 & CO2 3b. 03, S(CH3)2 ОН 4. Molecule W has the molecular formula C8H14. When Molecule W is reacted first with BHz in tetrahydrofuran (THF) then treated with basic hydrogen peroxide the resulting products are an optically inactive...
Unknown molecule with molecular formula C6H120. Which of these five molecules is it most likely to...
Unknown molecule with molecular formula C6H120. Which of these five molecules is it most likely to be? | Oo now od CH,20 3000 2000 Wavenumber (cm-1) 1000
Please help!! 7. (0) An unknown molecule Y has a molecular formula of CsH1002, a broad...
Please help!!
7. (0) An unknown molecule Y has a molecular formula of CsH1002, a broad absorption in its IR spectrum from 3200 to 3550 cm region, and no absorption in the 1620 to 1780 cm region. No carbon atom in the structure Y has more than one oxygen atom bonded to it and Y can exist in two (and only two) stereoisomeric forms. What are the structures of these forms of Y?
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...
Please help me! 7. (0) An unknown molecule Y has a molecular formula of CsH1002, a broad absorption in its IR spectr...
Please help me!
7. (0) An unknown molecule Y has a molecular formula of CsH1002, a broad absorption in its IR spectrum from 3200 to 3550 cm region, and no absorption in the 1620 to 1780 cm region. No carbon atom in the structure Y has more than one oxygen atom bonded to it and Y can exist in two (and only two) stereoisomeric forms. What are the structures of these forms of Y?
You have discovered an unknown molecule A. Oxidation with periodic acid furnishes two moles of carbon...
You have discovered an unknown molecule A. Oxidation with periodic acid furnishes two moles of carbon dioxide, 2 moles of formic acid and 2 moles of formaldehyde. Give a structure of a molecule that could be molecule A. Give four different ways to make acetone. You must use four different functional groups as your starting materials. Write the structures of all the constitutionally isomeric ethers of molecular formula C6H14O and give an acceptable name for each one.
A hydrocarbon of unknown structure g tHIS Intormation to answer questions 13-14 has the formula CgHz4....
A hydrocarbon of unknown structure g tHIS Intormation to answer questions 13-14 has the formula CgHz4. Upon hydrogenation over Pd/CaCO3, the molecule does not absorb hydrogen. Upon treatment with acidic aqueous KMn04 the following products are obtained in equal amounts. H3C CH CO2H Acetic Acid ???? 13. How many carbon-carbon triple bonds are in the molecule? (4 points) A. None B. One C. Two D. Three 14. Which of the following is the likely structure for the molecule (8 points)?...
4. Molecule W has the molecular formula C&H. When Molecule W is reacted first with BH3 in tetrahydrofuran (THF) then treated with basic hydrogen peroxide the resulting products are an optically inactive mixture of molecules H and A. When molecule Wis treated with warm KMnO4 followed by an acidic water treatment the molecule below is the product. Draw out the structure for molecules W. H and A? You must show all of your work in order to earn full credit...
. When Molecule W is reacted first with cules H and A. When molecule Wis 4. Molecule W has the molecular formula C8H14. When Molecule W is reaca BH3 in tetrahydrofuran (THF) then treated with basic hydrogen peroxide the resu eroxide the resulting products are an optically inactive mixture of molecules H and A. When more treated with warm KMnO4 followed by an acidic water treatment the molecule the product. Draw out the structure for molecules W, H and A?...
6. An organic compound U with molecular formula C19H38 gave 2, 6, 12, 14- tetramethylpentadecane on hydrogenation. Ozonolysis of U gave propanone and a 16- carbon aldehyde V as products. Give the structures of U and V and provide the name for U. 7. An unknown hydrocarbon Q has a formula CaH12. Q Reacts with osmium tetroxide to give a diol R. When oxidized with KM O4 in an acidic medium, Q gives two products. One product is propanoic acid...
i'm having trouble going backwards in reactions. if you have
any tips please share. thank you!
3. For each reaction determine the reactant that lead to the formation of the indicated products. (3 points each) 3a. 1. KMnO4, warm 2. H, H20 & CO2 3b. 03, S(CH3)2 ОН 4. Molecule W has the molecular formula C8H14. When Molecule W is reacted first with BHz in tetrahydrofuran (THF) then treated with basic hydrogen peroxide the resulting products are an optically inactive...
Unknown molecule with molecular formula C6H120. Which of these five molecules is it most likely to be? | Oo now od CH,20 3000 2000 Wavenumber (cm-1) 1000
Please help!!
7. (0) An unknown molecule Y has a molecular formula of CsH1002, a broad absorption in its IR spectrum from 3200 to 3550 cm region, and no absorption in the 1620 to 1780 cm region. No carbon atom in the structure Y has more than one oxygen atom bonded to it and Y can exist in two (and only two) stereoisomeric forms. What are the structures of these forms of Y?
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...
Please help me!
7. (0) An unknown molecule Y has a molecular formula of CsH1002, a broad absorption in its IR spectrum from 3200 to 3550 cm region, and no absorption in the 1620 to 1780 cm region. No carbon atom in the structure Y has more than one oxygen atom bonded to it and Y can exist in two (and only two) stereoisomeric forms. What are the structures of these forms of Y?
A hydrocarbon of unknown structure g tHIS Intormation to answer questions 13-14 has the formula CgHz4. Upon hydrogenation over Pd/CaCO3, the molecule does not absorb hydrogen. Upon treatment with acidic aqueous KMn04 the following products are obtained in equal amounts. H3C CH CO2H Acetic Acid ???? 13. How many carbon-carbon triple bonds are in the molecule? (4 points) A. None B. One C. Two D. Three 14. Which of the following is the likely structure for the molecule (8 points)?...
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