Homework Answers
The molecule of acetanilide contains three different hydrogens. They are:-
The methyl hydrogens:-
They are the hydrogen which is attached to the carbon forming methyl group. The methyl group is attached to the C=O of amide group. These hydrogens will be occur at nearly 2 ppm as they dont face any kind of distortion by an electronegative atom.
The hydrogen attached to nitrogen:-
This hydrogen is highly acidic as it is attached to an electronegative atom. The hydrogen atom will appear at downfield as greater distortion by the nitrogen atom takes place. Since, 1H peak near 8 ppm resonates with this hydrogen.
The hydrogens in the benzene ring.
They occur as multiplet and around 7.5-6 ppm. They occur at little downfield than methyl hydrogens as they are attached to sp2 carbons which result in greater distortion.
Thus,
Hydrogens a, b and c corresponds to peak 2.
Hydrogen d corresponds to peak 1.
Hydrogen e corresponds to peak 3.
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Question 8 (5 points) Saved Acetanilide: Match the peaks to the appropriate number on the structure....
Thank you for your help! Question 9 (6 points) Seved Acetanilide: Match the peaks to the...
Thank you for your help!
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match the name to the IR structure and justify (name peaks) it. the numbers are the...
match the name to the IR structure and justify (name peaks)
it.
the numbers are the same on all graphs going:
4800....3000...2000....1500...1000...500
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Thank you for your help!
Question 9 (6 points) Seved Acetanilide: Match the peaks to the appropriate number on the structure. A letter may correspond to more than one number. TTTTTTTT 200 180 160 140 120 100 80 60 200 180 160 140 120 100 80 60 40 20 0 3 2. 2 3. 3 4. 4 5. 5
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match the name to the IR structure and justify (name peaks)
it.
the numbers are the same on all graphs going:
4800....3000...2000....1500...1000...500
Names of possible structures: propanoic anhydride 3-methyl-3-buten-1-ol 1,3,5-trimethylbenzene propanenitrile hexanoyl chloride N,N-dimethylformamide isopropanol hex-l-yne butyramide cyclohexylamine Ethyl propionate oct-4-yne 1. 100 8 TENSMETTANCER +0 000 0006 2000 1500 TENSMETTENCER 8 510 3. LP 30.00 OST BERI 001 mi 000 110 MENERI 001 5. 4100 3000 6. 흘 Cog 000 VENUE 100 7. tood 100 100 EUR 10. 11....
Spectroscopy of C5H10O
1. Correctly label 2 peaks in the IR spectrum with the appropriate functional group. 2. Correctly label 1 peak in the 13C NMR spectrum. 3. Draw some possible structures (isomers) as you analyze the 'H NMR spectrum. 4. Draw your final choice of structure to match the IR. 13C NMR, and H NMR 5. Label the different types of hydrogens on your structure as a, b, c, etc. Label the peaks in the 'H NMR spectrum with...
frog structure 2
QUESTION 10 Observe the dissected frog below 8 2 5 6 Image copied with permission. University of Wisconsin La Crosse Zoo-Lab Match the number labels with the appropriate frog structure a.)3 a. Large intestines.com b. Stomach - sac-like org Lungs- respiration C. b. 11 214 Click Save and Submit to save and submit Click Save As To all answers, étv
Question 5 (3 points) After drawing the Lewis dot structure for XeCl4, determine the number of single bonds, double bonds, and lone pairs on the central atom. 4,0,0 O 1, 3,0 4,0,2 3,1,0 4.0,1 into Saved
5) Assign the peaks in the 'H NMR spectrum of your product. Draw your structure on the NMR spectrum and label each set of inequivalent protons. Use these labels in assigning the peaks. In some cases the aromatic peaks may overlap, so it is OK to assign groups of protons to a series of overlapping peaks if necessary. Try to be as specific as possible in your assignment, though. Discuss in detail how the NMR spectrum is only consistent with...
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