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Concept explainers
Interpretation:
The reason for the higher boiling point of ethylene glycol as compared to propanol and a compound with a similar molar mass is to be determined.
Concept introduction:
Intermolecular forces operate between the molecules so changes with change in the phase and effects with physical properties of the substance. In intermolecular forces, the bond is formed between two molecules with partial charges that are present relatively far away from each other. The types of intermolecular forces are as follows:
1. Ion-dipole: Ion-dipole forces are the attractive forces that exist between an ion and a polar molecule.
2. Hydrogen bond: Hydrogen bonding is the attractive forces that exist between the molecule with a hydrogen atom bonded to an electronegative atom like fluorine, nitrogen, and oxygen of one molecule and an electronegative atom of another molecule.
3. Dipole-dipole: Dipole-dipole is the attractive forces that exist between two polar molecules that have a permanent dipole.
4. Ion-induced dipole: Ion-induced dipole is the attractive forces that exist between the ion and a nonpolar molecule.
5. Dipole-induced dipole: Dipole-induced dipole is the attractive forces that exist between a polar and a nonpolar molecule.
6. Dispersion forces: In dispersion forces, a temporary dipole is generated on one molecule that further induces a temporary dipole on the molecule adjacent to it. The temporary dipole results in the attraction between opposite charges and dispersion forces exist in the molecule. All the atoms and molecules exhibit dispersion forces.
The boiling point of the liquid is defined as the temperature at which the liquid and gas are in equilibrium and the pressure is
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Chapter 12 Solutions
Chemistry: The Molecular Nature of Matter and Change
- Draw a Newman projection from carbon 3 to carbon 2 in the highest energy conformation for the following molecule. What is this conformation called? What kind of strain is present? Brarrow_forwardWhich of the following dienophiles is most reactive in a Diels-Alder reaction: Please explain why the correct answer to this question is option 5. Please provide a detailed explanation.arrow_forwardWhich of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forward
- Draw the enantiomer and diastereomers of the following molecule. Label each type of stereoisomers. Label each chiral center as R or S. HOarrow_forwardWhich diene and dienophile would you choose to synthesize the following compound? Please provide a detailed explanation. Please include a drawing showing the mechanism of the synthesis. Please also explain why it is the correct diene and dienophile.arrow_forwardUsing the sketcher below, draw the structure of N-ethyldecylamine. Answer: 0 ୨୫) . 始 {n [ ]t ?arrow_forward
- Which of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forwardIdentify the characteristic signals that you would expect in the diagnostic region of an IR spectrum of each of the following compounds. a. H₂N b.arrow_forwardWhat is the lowest energy chair for the following cyclohexane? ' || || a. b. " " d.arrow_forward
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