The infrared spectrum for methanol. CH 3 OH, is illustrated below. It shows the amount of light in the infrared region that methanol transmits as a function of wavelength. The vertical axis is the amount of light transmitted. At points near the top of the graph, most of the incident light is being transmitted by the sample (or, conversely, little light is absorbed). Therefore, the ″peaks″ or ″bands″ that descend from the top indicate light absorbed; the longer the band, the more light is being absorbed. The horizontal scale is in units of ″wavenumbers,″ abbreviated cm −1 . The energy of light is given by Planck′s law as E = hc /λ; that is, E is proportional to 1/λ. Therefore, the horizontal scale is in units of 1/λ and reflects the energy of the light incident on the sample. (a) One point on the horizontal axis is marked as 2000 cm −1 . What is the wavelength of light at this point? (b) Which is the low energy end of this spectrum (left or right), and which is the high energy end? (c) The broad absorption at about 3300-3400 cm −1 indicates that infrared radiation is interacting with the OH group of the methanol molecule. The narrower absorptions around 2800-3000 cm −1 are for interactions with C—H bonds. Which interaction requires more energy, with O—H or with C—H?
The infrared spectrum for methanol. CH 3 OH, is illustrated below. It shows the amount of light in the infrared region that methanol transmits as a function of wavelength. The vertical axis is the amount of light transmitted. At points near the top of the graph, most of the incident light is being transmitted by the sample (or, conversely, little light is absorbed). Therefore, the ″peaks″ or ″bands″ that descend from the top indicate light absorbed; the longer the band, the more light is being absorbed. The horizontal scale is in units of ″wavenumbers,″ abbreviated cm −1 . The energy of light is given by Planck′s law as E = hc /λ; that is, E is proportional to 1/λ. Therefore, the horizontal scale is in units of 1/λ and reflects the energy of the light incident on the sample. (a) One point on the horizontal axis is marked as 2000 cm −1 . What is the wavelength of light at this point? (b) Which is the low energy end of this spectrum (left or right), and which is the high energy end? (c) The broad absorption at about 3300-3400 cm −1 indicates that infrared radiation is interacting with the OH group of the methanol molecule. The narrower absorptions around 2800-3000 cm −1 are for interactions with C—H bonds. Which interaction requires more energy, with O—H or with C—H?
The infrared spectrum for methanol. CH3OH, is illustrated below. It shows the amount of light in the infrared region that methanol transmits as a function of wavelength. The vertical axis is the amount of light transmitted. At points near the top of the graph, most of the incident light is being transmitted by the sample (or, conversely, little light is absorbed). Therefore, the ″peaks″ or ″bands″ that descend from the top indicate light absorbed; the longer the band, the more light is being absorbed. The horizontal scale is in units of ″wavenumbers,″ abbreviated cm−1. The energy of light is given by Planck′s law as E = hc/λ; that is, E is proportional to 1/λ. Therefore, the horizontal scale is in units of 1/λ and reflects the energy of the light incident on the sample.
(a) One point on the horizontal axis is marked as 2000 cm−1. What is the wavelength of light at this point?
(b) Which is the low energy end of this spectrum (left or right), and which is the high energy end?
(c) The broad absorption at about 3300-3400 cm−1 indicates that infrared radiation is interacting with the OH group of the methanol molecule. The narrower absorptions around 2800-3000 cm−1 are for interactions with C—H bonds. Which interaction requires more energy, with O—H or with C—H?
Calculate the proton and carbon chemical shifts for this structure
A.
B.
b. Now consider the two bicyclic molecules A. and B. Note that A. is a dianion
and B. is a neutral molecule. One of these molecules is a highly reactive
compound first characterized in frozen noble gas matrices, that self-reacts
rapidly at temperatures above liquid nitrogen temperature. The other
compound was isolated at room temperature in the early 1960s, and is a
stable ligand used in organometallic chemistry. Which molecule is the more
stable molecule, and why?
Where are the chiral centers in this molecule? Also is this compound meso yes or no?
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Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell