The molecular ion S 3 N 3 − has the cyclic structure All S − N bonds are equivalent. (a) Give six equivalent resonance hybrid Lewis diagrams for this molecular ion. (b) Compute the formal charges on all atoms in the molecular ion in each of the six Lewis diagrams. (c) Determine the charge on each atom in the polyatomic ion, assuming that the true distribution of electrons is the average of the six Lewis diagrams arrived at in parts (a) and (b). (d) An advanced calculation suggests that the actual charge resident on each N atom is − 0. 375 and on each S atom is + 0.0 41 . Show that this result is consistent with the overall + 1 charge on the molecular ion.
The molecular ion S 3 N 3 − has the cyclic structure All S − N bonds are equivalent. (a) Give six equivalent resonance hybrid Lewis diagrams for this molecular ion. (b) Compute the formal charges on all atoms in the molecular ion in each of the six Lewis diagrams. (c) Determine the charge on each atom in the polyatomic ion, assuming that the true distribution of electrons is the average of the six Lewis diagrams arrived at in parts (a) and (b). (d) An advanced calculation suggests that the actual charge resident on each N atom is − 0. 375 and on each S atom is + 0.0 41 . Show that this result is consistent with the overall + 1 charge on the molecular ion.
The molecular ion
S
3
N
3
−
has the cyclic structure
All
S
−
N
bonds are equivalent.
(a) Give six equivalent resonance hybrid Lewis diagrams for this molecular ion.
(b) Compute the formal charges on all atoms in the molecular ion in each of the six Lewis diagrams.
(c) Determine the charge on each atom in the polyatomic ion, assuming that the true distribution of electrons is the average of the six Lewis diagrams arrived at in parts (a) and (b).
(d) An advanced calculation suggests that the actual charge resident on each N atom is
−
0.
375
and on each S atom is
+
0.0
41
. Show that this result is consistent with the overall
+
1
charge on the molecular ion.
Please help me calculate the undiluted samples ppm concentration.
My calculations were 280.11 ppm. Please see if I did my math correctly using the following standard curve.
Link: https://mnscu-my.sharepoint.com/:x:/g/personal/vi2163ss_go_minnstate_edu/EVSJL_W0qrxMkUjK2J3xMUEBHDu0UM1vPKQ-bc9HTcYXDQ?e=hVuPC4
Provide an IUPAC name for each of the compounds shown.
(Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to
commas, dashes, etc.)
H₁₂C
C(CH3)3
C=C
H3C
CH3
CH3CH2CH
CI
CH3
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Arrange the following compounds / ions in increasing nucleophilicity (least to
most nucleophilic)
CH3NH2
CH3C=C:
CH3COO
1
2
3
5
Multiple Choice 1 point
1, 2, 3
2, 1, 3
3, 1, 2
2, 3, 1
The other answers are not correct
0000
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Quantum Molecular Orbital Theory (PChem Lecture: LCAO and gerade ungerade orbitals); Author: Prof Melko;https://www.youtube.com/watch?v=l59CGEstSGU;License: Standard YouTube License, CC-BY