(a)
Interpretation:
Consider the compounds,
Concept introduction:
Intermolecular forces are Van der Waals forces. They are weak and have threetypes viz., London dispersion forces, dipole-dipole forces and hydrogen bonding. Hydrogen bonding is relatively the strongest one.
- Intermolecular forces are the forces acting between molecules whereas Intramolecular forces are the forces that operate within a molecule.
- Hydrogen bonding is a special type of Dipole-dipole forces but stronger than the former.
- London dispersion forces exist in non-polar covalent compounds whereas dipole-dipole forces exist in polar covalent compounds but both are weak.
- Larger the molecular size, stronger the London dispersion force.
- Arrangement of major types of intermolecular forces in increasing order of strength:
There exist no deviations in this arrangement.
(a)
Explanation of Solution
Intermolecular force in each compound
In a 1-Pentanol, the intermolecular forces are London forces, dipole-dipole forces and hydrogen bonding, whereas only London forces are present in Hexane.
(b)
Interpretation:
Consider the compounds,
Concept introduction:
Intermolecular forces are Van der Waals forces. They are weak and have threetypes viz., London dispersion forces, dipole-dipole forces and hydrogen bonding. Hydrogen bonding is relatively the strongest one.
- Intermolecular forces are the forces acting between molecules whereas Intramolecular forces are the forces that operate within a molecule.
- Hydrogen bonding is a special type of Dipole-dipole forces but stronger than the former.
- London dispersion forces exist in non-polar covalent compounds whereas dipole-dipole forces exist in polar covalent compounds but both are weak.
- Larger the molecular size, stronger the London dispersion force.
- Arrangement of major types of intermolecular forces in increasing order of strength:
There exist no deviations in this arrangement.
(b)
Explanation of Solution
Boiling point increases with increasing intermolecular forces. Hence, 1-Pentanol has higher intermolecular forces and hence it has higher boiling point. Thus Hexane has low boiling point due to its low intermolecular forces. That is the boiling point would be
(c)
Interpretation:
Consider the compounds,
Concept introduction:
Intermolecular forces are Van der Waals forces. They are weak and have threetypes viz., London dispersion forces, dipole-dipole forces and hydrogen bonding. Hydrogen bonding is relatively the strongest one.
- Intermolecular forces are the forces acting between molecules whereas Intramolecular forces are the forces that operate within a molecule.
- Hydrogen bonding is a special type of Dipole-dipole forces but stronger than the former.
- London dispersion forces exist in non-polar covalent compounds whereas dipole-dipole forces exist in polar covalent compounds but both are weak.
- Larger the molecular size, stronger the London dispersion force.
- Arrangement of major types of intermolecular forces in increasing order of strength:
There exist no deviations in this arrangement.
(c)
Explanation of Solution
To assign: viscosities of each compound
Viscosity increases with increasing intermolecular forces. Hence, 1-Pentanol has higher intermolecular forces and viscosity of this compound should be
(d)
Interpretation:
Consider the compounds,
Concept introduction:
Intermolecular forces are Van der Waals forces. They are weak and have threetypes viz., London dispersion forces, dipole-dipole forces and hydrogen bonding. Hydrogen bonding is relatively the strongest one.
- Intermolecular forces are the forces acting between molecules whereas Intramolecular forces are the forces that operate within a molecule.
- Hydrogen bonding is a special type of Dipole-dipole forces but stronger than the former.
- London dispersion forces exist in non-polar covalent compounds whereas dipole-dipole forces exist in polar covalent compounds but both are weak.
- Larger the molecular size, stronger the London dispersion force.
- Arrangement of major types of intermolecular forces in increasing order of strength:
There exist no deviations in this arrangement.
(d)
Explanation of Solution
To identify: boiling point of
The compound
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Chapter 11 Solutions
OWLv2 with Student Solutions Manual eBook for Ebbing/Gammon's General Chemistry, 11th Edition, [Instant Access], 4 terms (24 months)
- Please correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forward(11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B Bond A Bond C a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest Bond Strongest Bond b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. c. (5pts) Use principles discussed in lecture, supported by relevant structures, to succinctly explain the why your part b (i) radical is more stable than your part b(ii) radical. Written explanation can be no more than one-two succinct sentence(s)!arrow_forward
- . 3°C with TH 12. (10pts total) Provide the major product for each reaction depicted below. If no reaction occurs write NR. Assume heat dissipation is carefully controlled in the fluorine reaction. 3H 24 total (30) 24 21 2h • 6H total ● 8H total 34 래 Br2 hv major product will be most Substituted 12 hv Br NR I too weak of a participate in P-1 F₂ hv Statistically most favored product will be major = most subst = thermo favored hydrogen atom abstractor to LL Farrow_forwardFive chemistry project topic that does not involve practicalarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
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