a.
To predict:
The solubility, insolubility or the micelle formation property of Heptane on the basis of its polarity and attractive forces.
Introduction:
Molecules with similar polarity dissolve each other. The force that acts between the molecules which causes the interaction between them is called attractive forces.
b.
To predict:
The solubility, insolubility or the micelle formation property of Heptane on the basis of its polarity and attractive forces.
Introduction:
Molecules with similar polarity dissolve each other. The force that acts between the molecules which causes the interaction between them is called attractive forces.
c.
To predict:
The solubility, insolubility and micelle formation property of Heptane on the basis of its polarity and attractive forces.
Introduction:
Molecules with similar polarity dissolve each other. The force that acts between the molecules which causes the interaction between them is called attractive forces.
Want to see the full answer?
Check out a sample textbook solutionChapter 7 Solutions
General, Organic, and Biological Chemistry (3rd Edition)
- 9C.2 Some chemical reactions proceed by the initial loss or transfer of an electron to adiatomic species. Which of the following molecules would you expect to be stabilized by theaddition of an electron or the removal of an electron? N2, NO, O2, C2, F2, CN Before solving the problem please also give a brief explanation of the concept or associated equation(s) and variables. (In answer show and explain the sigma and pi bonds with electrons as should be used to help solve with that little graphic or what not) Also do not do something like NONO or N2N2 for your solution as that is not what the question is asking.arrow_forwardPlease correct answer and don't used hand raitingarrow_forwardNonearrow_forward
- Nonearrow_forward9.26 Explain in detail how you would distinguish between the following sets of compounds using the indicated method of spectroscopy. 1H NMR 13 C and 1H NMR 13C NMRarrow_forward9.21 How many 13C NMR signals would you predict for each of the compounds shown in Problem 9.20? OH Br OHarrow_forward
- Which of the following would be the expected major product and why? HCI CI II CI Product I because of resonance stabilization of the carbocation intermediate Product II because of resonance stabilization of the carbocation intermediate Product I because of inductive stabilization of the carbocation intermediate Product II because of inductive stabilization of the carbocation intermediatearrow_forwardNonearrow_forward9.20 How many ¹H NMR signals (not peaks) would you predict for each of the following compounds? (Consider all protons that would be chemical shift nonequivalent.) OH Br OHarrow_forward
- 9.22 Propose a structure for an alcohol with molecular formula C5H12O that has the 1H NMR spectrum given in Figurearrow_forwardFor each set of carbonyl additions, circle the carbonyl addition that occurs at the faster rate (assuming everything is the same except that the reagent/substrate differs - i.e., same temperature, and ratios/concentrations of reagent and substrate). Electrostatic attraction has a greater impact on the relative rates than steric hindrance. (a) CH3OH HO OCH3 H H CH3 i CH₂OH HO OCH 3 H F3C CH3 (b) F3C NaOCH3 HO OCH3 H3C CH3 H3C CH3 CH3OH HO OCH3 H3C CH3 H3C CH3 (c) NaSCH3 OSCH 3 H3C CH3 H3C CH3 NaOCH3 O OCH 3 H3C CH3 H3C CH3arrow_forward9.34. Assign the chemical shifts and splitting patterns to specific aspects of the structure you propose. C5H12O 1H 2H 2 6H ille H(ppm) 1 3H и 0arrow_forward
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning