[Review Topics] The functional groups in an organic compound can frequently be deduced from Its Infrared absorption spectrum. A compound containing C, H, and O exhibits broad absorption at 3450 cm-¹ (m) and an intense band at 1725, plus a band at 1100 cm-¹ (m). Relative absorption intensity: (s)=strong, (m)=medium, (w)=weak. What functional class(es) does the compound belong to? List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly. Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like 10 to 20 cm-¹. The functional class(es) of this compound is (are) spaces or commas.) a. alkane (List only if no other functional class applies.) b. alkene c. terminal alkyne d. internal alkyne e. arene f. 'alcohol g. ether [References] Submit Answer (Enter letters from the table below, in any order, with no h. amine i. aldehyde or ketone j. carboxylic acid k. ester I. nitrile Retry Entire Group 9 more group attempts remaining
[Review Topics] The functional groups in an organic compound can frequently be deduced from Its Infrared absorption spectrum. A compound containing C, H, and O exhibits broad absorption at 3450 cm-¹ (m) and an intense band at 1725, plus a band at 1100 cm-¹ (m). Relative absorption intensity: (s)=strong, (m)=medium, (w)=weak. What functional class(es) does the compound belong to? List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly. Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like 10 to 20 cm-¹. The functional class(es) of this compound is (are) spaces or commas.) a. alkane (List only if no other functional class applies.) b. alkene c. terminal alkyne d. internal alkyne e. arene f. 'alcohol g. ether [References] Submit Answer (Enter letters from the table below, in any order, with no h. amine i. aldehyde or ketone j. carboxylic acid k. ester I. nitrile Retry Entire Group 9 more group attempts remaining
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Concept explainers
Analyzing Infrared Spectra
The electromagnetic radiation or frequency is classified into radio-waves, micro-waves, infrared, visible, ultraviolet, X-rays and gamma rays. The infrared spectra emission refers to the portion between the visible and the microwave areas of electromagnetic spectrum. This spectral area is usually divided into three parts, near infrared (14,290 – 4000 cm-1), mid infrared (4000 – 400 cm-1), and far infrared (700 – 200 cm-1), respectively. The number set is the number of the wave (cm-1).
IR Spectrum Of Cyclohexanone
It is the analysis of the structure of cyclohexaone using IR data interpretation.
IR Spectrum Of Anisole
Interpretation of anisole using IR spectrum obtained from IR analysis.
IR Spectroscopy
Infrared (IR) or vibrational spectroscopy is a method used for analyzing the particle's vibratory transformations. This is one of the very popular spectroscopic approaches employed by inorganic as well as organic laboratories because it is helpful in evaluating and distinguishing the frameworks of the molecules. The infra-red spectroscopy process or procedure is carried out using a tool called an infrared spectrometer to obtain an infrared spectral (or spectrophotometer).
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[Review Topics]
[References]
The functional groups in an organic compound can frequently be deduced from Its Infrared absorption spectrum. A
compound containing C, H, and O exhibits broad absorption at 3450 cm-¹ (m) and an intense band at
1725, plus a band at 1100 cm-¹ (m).
Relative absorption intensity: (s)=strong, (m)=medium, (w)=weak.
What functional class(es) does the compound belong to?
List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly.
Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like
10 to 20 cm-¹.
The functional class(es) of this compound is (are)
spaces or commas.)
a. alkane (List only if no other functional class applies.)
b. alkene
c. terminal alkyne
d. internal alkyne
e. arene
f. 'alcohol
g. ether
Submit Answer
2
(Enter letters from the table below, in any order, with no
h. amine
i. aldehyde or ketone
j. carboxylic acid
k. ester
I. nitrile
Retry Entire Group 9 more group attempts remaining
AO
Tp S
for
W
*
Previous
Email Instructor
Next>
Upd
Save and Exit
Show All](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb28f2355-1ee4-45af-9977-578e8e77bde7%2F7cce6920-a111-4426-bfe5-af65b103d951%2Fqtdgzi8_processed.jpeg&w=3840&q=75)
Transcribed Image Text:n/takeAssignment/takeCovalent Activity.do?locator-assignment-take
M
2req
[Review Topics]
[References]
The functional groups in an organic compound can frequently be deduced from Its Infrared absorption spectrum. A
compound containing C, H, and O exhibits broad absorption at 3450 cm-¹ (m) and an intense band at
1725, plus a band at 1100 cm-¹ (m).
Relative absorption intensity: (s)=strong, (m)=medium, (w)=weak.
What functional class(es) does the compound belong to?
List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly.
Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like
10 to 20 cm-¹.
The functional class(es) of this compound is (are)
spaces or commas.)
a. alkane (List only if no other functional class applies.)
b. alkene
c. terminal alkyne
d. internal alkyne
e. arene
f. 'alcohol
g. ether
Submit Answer
2
(Enter letters from the table below, in any order, with no
h. amine
i. aldehyde or ketone
j. carboxylic acid
k. ester
I. nitrile
Retry Entire Group 9 more group attempts remaining
AO
Tp S
for
W
*
Previous
Email Instructor
Next>
Upd
Save and Exit
Show All
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