If a compound had 4 degrees of unsaturation, which set of conditions is NOT possible for...
If a compound had 4 degrees of unsaturation, which set of conditions is NOT possible for the structure?
A. One triple bond, one double bond
B. One triple bond, two rings
C. Two rings and two double bonds
D. One triple bond, one double bond, one ring
Homework Answers
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If a compound had 4 degrees of unsaturation, which set of
conditions is NOT possible for...
MULTIPLE CHOICE. 1) W Choose the on e alternative that best completes the statement or answers...
MULTIPLE CHOICE. 1) W Choose the on e alternative that best completes the statement or answers the question. hat possible structures does a compound with molecular formula CoHio have? A) three rings, three double bonds, two double bonds + one ring, one ring + or one double bond + one ring B) one double bond and no rings one ring two double bonds, one triple bond + two rings, two double bonds, one double bond + one ring or one...
For the following formula, CsHo, calculate the IHD and select all the types of unsaturation that...
For the following formula, CsHo, calculate the IHD and select all the types of unsaturation that might be present in the molecule based on the IHD. Number IHD= The types of unsaturation that might be present: no unsaturation; no multiple bonds or ring closings one double bond or one ring closing three double bonds or three ring closings; or two double bonds and one ring closing; or one double bond and two ring closings; or one triple bond and one...
1. Index of hydrogen deficiency (IHD)/ degree of unsaturation will tell us the total number of...
1. Index of hydrogen deficiency (IHD)/ degree of unsaturation will tell us the total number of rings and pi bonds in a molecule. Although the final structure can only be verified by IR/NMR spectra, if molecular formula is known, 1HD may be calculated and this will aive us an initial hint about the structure of an unknown molecule. HD is given by following equation: 2C + 2-H +N-X # carbons, H = # hydrogens, IHD = where, C N= #Nitrogens...
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 explain all answers! MC.4 A compound X with molecular formula CgHı2 and no triple bonds...
please explain all answers!
MC.4 A compound X with molecular formula CgHı2 and no triple bonds reacts with one equivalent of H2 to give a new compound having molecular formula C2H4. What can be said about the structure of compound X? A) Compound X has 3 rings. B) Compound X has 1 ring and 2 double bonds. Compound X has 2 rings and 1 double bond. Compound X has 3 double bonds. It's impossible to say anything about the structure...
please explain how you got it. i for every carbon their needs to be 2 hydrogen,...
please explain how you got it. i for every carbon their needs to be
2 hydrogen, so does that have anything to do with it?
3. Consider molecules with the formula C10H16. Which of the following structural features are not possible within this set of molecules? A. 2 triple bonds B. 1 ring and 1 triple bond C. 2 rings and 1 double bond D. 2 double bonds and 1 ring E. 3 double bonds
Calculate the degrees of unsaturation in a compound with the molecular formula CsHs and draw two possible structure...
Calculate the degrees of unsaturation in a compound with the molecular formula CsHs and draw two possible structures, including hydrogen atoms, for the formula. Number Degrees of unsaturation: In Up & View Solution Check Answer Next Ext
Chapter 7: Alkenes: Structure and Reactivity Degrees of unsaturation briple bond. DOU- 1. Calculate degrees of...
Chapter 7: Alkenes: Structure and Reactivity Degrees of unsaturation briple bond. DOU- 1. Calculate degrees of unsaturation in the following formulas: DOU = C+1+ NP - H,F,CI, Br, 1 I DOUS1 doune bondy (a) CHI 10+1 -1 16 = 3 Liring (b) C.H. 4 (e) CH20 (d) C&H BINO - C2H4O2 Jive IUPAC names for following alkenes: Prenti loncest chan containing alkee na shaun must contain double bond lauest double bond -ere 12
Choices: degrees of saturation: 0,1, 2, or, 3 Cardi B prepares compound D according the scheme below. Cardi B enjoys t...
Choices: degrees of saturation: 0,1, 2, or,
3
Cardi B prepares compound D according the scheme below. Cardi B enjoys the odor of compound D, which recalls the refreshing sting of ammonia or other disinfectant. SOCI 2 equiv NH LIAIH Compound A CeH1202 Compound C CgH13NO Compound D Compound B H2O Though Cardi is unwilling to provide you with the identity of D, she has provided the molecular formula and IR data of compound A and the molecula formula and...
C6H7ON Draw the molecule that corresponds to each. Make sure it matches 4 degrees of unsaturation....
C6H7ON Draw the molecule that corresponds to each. Make sure it matches 4 degrees of unsaturation. a. contains one nitrogen in trigonal planar b. contains one sp2 hybridized nitrogen and oxygen c. contains two sp hybridized atoms d. contains one ring Thank you! I am having trouble with these.
MULTIPLE CHOICE. 1) W Choose the on e alternative that best completes the statement or answers the question. hat possible structures does a compound with molecular formula CoHio have? A) three rings, three double bonds, two double bonds + one ring, one ring + or one double bond + one ring B) one double bond and no rings one ring two double bonds, one triple bond + two rings, two double bonds, one double bond + one ring or one...
For the following formula, CsHo, calculate the IHD and select all the types of unsaturation that might be present in the molecule based on the IHD. Number IHD= The types of unsaturation that might be present: no unsaturation; no multiple bonds or ring closings one double bond or one ring closing three double bonds or three ring closings; or two double bonds and one ring closing; or one double bond and two ring closings; or one triple bond and one...
1. Index of hydrogen deficiency (IHD)/ degree of unsaturation will tell us the total number of rings and pi bonds in a molecule. Although the final structure can only be verified by IR/NMR spectra, if molecular formula is known, 1HD may be calculated and this will aive us an initial hint about the structure of an unknown molecule. HD is given by following equation: 2C + 2-H +N-X # carbons, H = # hydrogens, IHD = where, C N= #Nitrogens...
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 explain all answers!
MC.4 A compound X with molecular formula CgHı2 and no triple bonds reacts with one equivalent of H2 to give a new compound having molecular formula C2H4. What can be said about the structure of compound X? A) Compound X has 3 rings. B) Compound X has 1 ring and 2 double bonds. Compound X has 2 rings and 1 double bond. Compound X has 3 double bonds. It's impossible to say anything about the structure...
please explain how you got it. i for every carbon their needs to be
2 hydrogen, so does that have anything to do with it?
3. Consider molecules with the formula C10H16. Which of the following structural features are not possible within this set of molecules? A. 2 triple bonds B. 1 ring and 1 triple bond C. 2 rings and 1 double bond D. 2 double bonds and 1 ring E. 3 double bonds
Calculate the degrees of unsaturation in a compound with the molecular formula CsHs and draw two possible structures, including hydrogen atoms, for the formula. Number Degrees of unsaturation: In Up & View Solution Check Answer Next Ext
Chapter 7: Alkenes: Structure and Reactivity Degrees of unsaturation briple bond. DOU- 1. Calculate degrees of unsaturation in the following formulas: DOU = C+1+ NP - H,F,CI, Br, 1 I DOUS1 doune bondy (a) CHI 10+1 -1 16 = 3 Liring (b) C.H. 4 (e) CH20 (d) C&H BINO - C2H4O2 Jive IUPAC names for following alkenes: Prenti loncest chan containing alkee na shaun must contain double bond lauest double bond -ere 12
Choices: degrees of saturation: 0,1, 2, or,
3
Cardi B prepares compound D according the scheme below. Cardi B enjoys the odor of compound D, which recalls the refreshing sting of ammonia or other disinfectant. SOCI 2 equiv NH LIAIH Compound A CeH1202 Compound C CgH13NO Compound D Compound B H2O Though Cardi is unwilling to provide you with the identity of D, she has provided the molecular formula and IR data of compound A and the molecula formula and...
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