Calculate the degrees of unsaturation in a compound with the molecular formula C3H6 and draw two possible structures, including hydrogen atoms, for the formula.
This problem is based on the concept of isomers.
Isomers that have same molecular formula but different arrangement of atoms in space or different bonding between atoms. Isomers have same molecular formulae but different chemical and physical properties.
Isomers can be determined easily if the molecular formula is known by using various methods like degree of unsaturation. Formula of degree of unsaturation is as follows:
Here, is number carbon atoms, is valency of carbon atom, is number of hydrogen atoms and is valency of hydrogen atom.
The given molecular formula is .
Degree of unsaturation
Substitute, 3 for , 4 for , 6 for and 1 for .
Structures of the compound having the molecular formula of are given below:
Ans:Degree of unsaturation for the molecular formula is 1.
The possible structures of the compound having the molecular formula of are given below:
Calculate the degrees of unsaturation in a compound with the molecular formula C3H6 and draw two...
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
1. Calculate the degrees of unsaturation (DOU) for the following molecular formulate and propose two possible structures for each formula: 1. Calculate the degrees of unsaturation (DOU) for the following molecular formulate and propose two possible structures for each formula: Formula DOU Structure 1 Structure 2 CeHeo C4H
Given the molecular formula calculate the degree of unsaturation for the following compound C8H9NO3. And what are three possible structures consistent with the degree of unsaturation for the compound?
Given the molecular formula, calculate the degree of unsaturation for the following compound. Suggest at least three possible structures consistent with the degree of unsaturation for each compound. (Special case: A nitro grou, -NO_2, has one degree of unsaturation. This information doesnt matter when you are calculating the degree of unsaturation, but it might matter when you start drawing structures.) C_3H_14O_2 C_2H_30 O C_5H_10 O C_4H_9NO_3 C_4H_4O_2 C_2H_10 Cl_2
Determine the degrees of unsaturation and draw a possible structure for the following molecular formula (5 points): 5. C16H24
5) [4 pts) Calculate the number of degrees of unsaturation for a molecule with molecular formula C9HgF3NO and draw two potential isomers. (2(c)+2-X+N)-H (2(9)+2-3+1)-8 .
2. For the following isotopic peak data, determine the molecular formula, calculate the degrees of unsaturation, and propose one possible structure: 2. For the following isotopic peak data, determine the molecular formula, calculate the degrees of unsaturation, and propose one possible structure: Peak Mass Relative Formula DOU Structure (MZ) Height (M)+. 87.105 100.0% (M+1)+. 88.108 5.4% The (M)" peak is an odd number. What does this tell you? B. Peak Formula DOU Structure Mass (MZ) Relative Height (M]+. 100.089 100.0%...
Calculate the molecular formula and the degrees of unsaturation of your unknown: Unknown C - 63.56502% H - 6.000798% N - 9.26604% O - 21.16814% Molar mass = 151
Compound A has the molecular formula C10H14. a) Calculate the unsaturation number or IHD. b) Provide the molecular ion observed in the mass spectrum, including its units. c) Propose a structure based on the carbon-13 NMR spectrum given. CH3 CH Compound A CDCl3 160 140 120100 80 60 40 20 0 CH3 CH Compound A CDCl3 160 140 120100 80 60 40 20 0
Diazomethane is an organic compound with molecular formula CH2N2. Draw the Lewis dot structure for this compound. Calculate the formal charges on the carbon and nitrogen atoms. Draw a resonance structure for this compound, using arrows to indicate flow of electrons. Are the two resonance structures identical? If not, indicate the major and minor contributors giving suitable explanation.