-1 An acidic liquid has a broad band at 3300 cm and a sharp band at 1710 cm-¹ in the infrared spectrum. One mole of this unknown reacts with one mole of NaOH. The ¹H NMR spectrum shows three peaks in the ratio 2 : 2:1. Microanalysis gave C, 33.2%; H, 4.6%; C1, 32.7%. Deduce the structure of the unknown. Spell out the full name of the compound.
-1 An acidic liquid has a broad band at 3300 cm and a sharp band at 1710 cm-¹ in the infrared spectrum. One mole of this unknown reacts with one mole of NaOH. The ¹H NMR spectrum shows three peaks in the ratio 2 : 2:1. Microanalysis gave C, 33.2%; H, 4.6%; C1, 32.7%. Deduce the structure of the unknown. Spell out the full name of the compound.
Chemistry
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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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![and
An acidic liquid has a broad band at 3300 cm
a sharp band at 1710 cm in the infrared spectrum.
One mole of this unknown reacts with one mole of
NaOH. The ¹H NMR spectrum shows three peaks
in the ratio 2 : 2 : 1. Microanalysis gave C, 33.2 %;
H, 4.6%; C1, 32.7%.
Deduce the structure of the unknown.
Spell out the full name of the compound.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fbbba6467-9518-4216-af68-86921dbd3664%2F3f256ff2-28fc-4be6-a52e-c66ff29d504d%2F7f572z5_processed.png&w=3840&q=75)
Transcribed Image Text:and
An acidic liquid has a broad band at 3300 cm
a sharp band at 1710 cm in the infrared spectrum.
One mole of this unknown reacts with one mole of
NaOH. The ¹H NMR spectrum shows three peaks
in the ratio 2 : 2 : 1. Microanalysis gave C, 33.2 %;
H, 4.6%; C1, 32.7%.
Deduce the structure of the unknown.
Spell out the full name of the compound.
![The product formed upon oxidation of an unknown
organic compound with chromic acid has the molecular
formula, C5 H10O. The ¹H NMR spectrum of the
product is shown below and its IR spectrum has a strong
band at 1700 cm-¹.(Figure 1)
Using this information, deduce the structure of the product and
hence the structure of the unknown compound.
Figure
3
2
1
<
1 of 1
ppm](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fbbba6467-9518-4216-af68-86921dbd3664%2F3f256ff2-28fc-4be6-a52e-c66ff29d504d%2Fh9tz8yq_processed.jpeg&w=3840&q=75)
Transcribed Image Text:The product formed upon oxidation of an unknown
organic compound with chromic acid has the molecular
formula, C5 H10O. The ¹H NMR spectrum of the
product is shown below and its IR spectrum has a strong
band at 1700 cm-¹.(Figure 1)
Using this information, deduce the structure of the product and
hence the structure of the unknown compound.
Figure
3
2
1
<
1 of 1
ppm
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