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Interpretation:
The reasons for butane to exist as gas and hexane as liquid at room temperature are to be determined.
Concept Introduction:
A hydrocarbon is organic compound consisting entirely of hydrogen and carbon.
Butane and hexane both are hydrocarbon. Butane is a four-carbon
The temperature at which the vapour pressure of the liquid is equal to the pressure exerted on the liquid by the surrounding atmosphere is called boiling point.
Boiling point of a molecule depends on the intermolecular forces and thermal energy.
Intermolecular forces are of two types: dispersion forces and dipole forces.
Dispersion forces are possessed by all the atoms or molecules, which depend on the molar mass.
Dipole forces exist between polar molecules, which depend on the polarity of the molecules.
Intermolecular forces keep the molecules together. Greater the intermolecular force, higher is the boiling point.
All atoms and molecules possess dispersion forces which depend upon their molar mass.
Polar molecules possess dipole forces between them which depend upon the polarity of the molecules.
A molecular formula consists of the
Dispersion forces are weak intermolecular forces and are considered van der waals forces.
Temporary dipoles can occur in non-polar molecules when the electrons that constantly orbit the nucleus occupy a similar location by chance.
Higher the molar mass, higher is the magnitude of the dispersion forces, and hence, higher is the boiling point.
Molecules which have lower molar masses have lower dispersion forces because dispersion force is directly proportional to the molar mass.
Molecules which have higher molar masses have higher dispersion forces.
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Chapter 12 Solutions
Bundle: Chemistry In Focus: A Molecular View Of Our World, 6th + Owlv2 6-month Printed Access Card
- Nonearrow_forwardDraw 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_forward
- Which of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forwardDraw 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_forward
- Using the sketcher below, draw the structure of N-ethyldecylamine. Answer: 0 ୨୫) . 始 {n [ ]t ?arrow_forwardWhich 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_forward
- What is the lowest energy chair for the following cyclohexane? ' || || a. b. " " d.arrow_forwardAnswer the following questions using the below figure: Potential Energy ри Reaction Progress a. How many transition states occur in this reaction? b. How many intermediates occur in this reaction? c. Is this reaction spontaneous or nonspontaneous? d. Does this reaction have a positive or negative AG? e. Label the activation energy(ies).arrow_forwardDraw the following molecule as a chair in the lowest energy conformation. Then perform a chair flip. Brarrow_forward
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