A certain hydrocarbon contains 11.12% of hydrogen by mass. Given that the molecular mass of the...
2:06 B A certain hydrocarbon contains 11.12% of hydrogen by mass. Given that the molecular mass of the hydrocarbon is 54, which of the following may be true about the compound? i. The compound can contain up to 2 double bonds per molecule ii. The compound can contain up to 2 rings per molecule iii. The compound can contain at most 1 triple bond. jij only O i & ii only O i only ii only O i, ii &...
When treated with excess hydrogen gas under catalytic condition, X mol of a certain hydrocarbon absorbed 11.2 L of hydrogen gas (measured at s.t.p). Which of the following is CORRECT? X = 0.25; the hydrocarbon is an alkene with two double bonds X = 1; the hydrocarbon is an alkyne with two triple bonds O X = 0.5; the hydrocarbon is an alkyne with one triple bond X = 0.5; the hydrocarbon is an alkene with two double bond X...
1) Draw the structure of a hydrocarbon that contains seven carbons with i. Aring and two double bonds i. Two rings and one double bond ii Three double bonds
2:21 B 81% Analysis by mass of a compound containing carbon, hydrogen, oxygen and nitrogen only showed that it contains 40.67% C, 8.47% H, and 23.73% N by mass. Given that the molecular mass of the compound is 59. Determine the possible number of double bonds plus rings in a molecule of the compound. [C=12, H=1, O=16, N=14] 3 1 4 0 2 What is the total number of stereoisomers possible for the compound shown above? OH w
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...
BONUS Question: (8) A sample of a hydrocarbon compound (contains only carbon and hydrogen) is known to consists of molecules having five carbon atoms. If the density of this hydrocarbon gas at STP conditions is 3.2215 grams/liter, what is the molecular formula for this compound?
Squalene, an important intermediate in the biosynthesis of steroids, has the molecular formula C30H50 and has no triple bonds. (a) What is the index of hydrogen deficiency of squalene? (b) Squalene undergoes catalytic hydrogenation to yield a compound with the molecular formula C30H62. How many double bonds does a molecule of squalene have? (c) How many rings?
30) 30) A compound X of molecular formula CgH12 with no triple bonds reacts with one equivalent of H2 to give a new compound having molecular formula CgH14. What can be inferred about the structure of compound X? A) Compound X has 2 rings and 1 p bond. B) Compound X has 3 p bonds. C) Compound X has 1 ring and 2 p bonds. D) Compound X has 3 rings. 31) Determine the product of the following reaction. Н....
matching chemistry Matching. Match the word to its definition. (1 point each) A. An uns carbonyl A. An unsaturated hydrocarbon that contains one or more group carbon-carbon triple bond. General formula C H2n-2 alkyl group B. A compound containing one or more benzene rings. conformation C. A compound that contains an -OH group bonded to a benzene ring. alkanes D. Any three-dimensional arrangement of atoms in a molecule A NOSSO OT that results from rotation about a single bond. alkenes...