(a)
Interpretation:
The stabilizing interactions between DMSO solvent molecules and a dissolved sodium ion are to be shown.
Concept introduction:
The dipole moment is defined as the charge separation between two atoms in a covalent bond or between two ions in an ionic bond. It is used to determine the polarity of atoms or ions. If the value of dipole moment is zero, then the molecule is said to be non-polar, and if the value of dipole moment is not zero, then the molecule is said to be polar and possess permanent dipole moment.
The solvent dimethyl sulfoxide (DMSO) is polar aprotic in nature. In the solution when an ionic compound is dissolved, this polar solvent shows charge-dipole interactions and donor interactions with it.
(b)
Interpretation:
The stabilizing interactions between DMSO solvent molecules and dissolved water are to be shown.
Concept introduction:
The dipole moment is defined as the charge separation between two atoms in a covalent bond or between two ions in an ionic bond. It is used to determine the polarity of atoms or ions. If the value of dipole moment is zero, then the molecule is said to be non-polar, and if the value of dipole moment is not zero, then the molecule is said to be polar and possess permanent dipole moment.
The solvent dimethyl sulfoxide (DMSO) is polar aprotic in nature. In the solution when an ionic compound is dissolved, this polar solvent shows charge-dipole interactions and donor interactions with it.
(c)
Interpretation:
The stabilizing interactions between DMSO solvent molecules and a dissolved chloride ion are to be shown.
Concept introduction:
The dipole moment is defined as the charge separation between two atoms in a covalent bond or between two ions in an ionic bond. It is used to determine the polarity of atoms or ions. If the value of dipole moment is zero, then the molecule is said to be non-polar, and if the value of dipole moment is not zero, then the molecule is said to be polar and possess permanent dipole moment.
The solvent dimethyl sulfoxide (DMSO) is polar aprotic in nature. In the solution when an ionic compound is dissolved, this polar solvent shows charge-dipole interactions and donor interactions with it.
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Chapter 8 Solutions
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
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- Part VII. Below are the 'HNMR, 13 C-NMR, COSY 2D- NMR, and HSQC 2D-NMR (similar with HETCOR but axes are reversed) spectra of an organic compound with molecular formula C6H1003 - Assign chemical shift values to the H and c atoms of the compound. Find the structure. Show complete solutions. Predicted 1H NMR Spectrum 4.7 4.6 4.5 4.4 4.3 4.2 4.1 4.0 3.9 3.8 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 f1 (ppm) Predicted 13C NMR Spectrum 100 f1 (ppm) 30 220 210 200 190 180 170 160 150 140 130 120 110 90 80 70 -26 60 50 40 46 30 20 115 10 1.0 0.9 0.8 0 -10arrow_forwardQ: Arrange BCC and Fec metals, in sequence from the Fable (Dr. R's slides) and Calculate Volume and Density. Aa BCC V 52 5 SFCCarrow_forwardNonearrow_forward
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