Question

QUESTION 2 1 pointsSave Answer Below are the IR spectrum of aldol on the left and the table for the list of stretching bonds

0 0
Add a comment Improve this question Transcribed image text
Answer #1

2. The frequency 1 of the IR spectra belongs to the =C-H stretch i.e, sp^2 C-H stretch. The stretching values occur at 3054.6 and 3057 cm^-1 (more than 3000cm^-1)

Correct option is 4 i.e, D - C(sp^2)-H stretch.

3. The frequency 3 occurs in pairs at around 1589 cm^-1 and 1573cm^-1.This occurs due to the (C=C) stretch of the aromatic ring.

The correct option is 4 i.e, K - C=C aromatic

4. The second frequency occurs at around 1650 cm^-1. This is due to the (C=C) stretch.

Correct option is 3 i.e, J - C=C stretch

Add a comment
Know the answer?
Add Answer to:
QUESTION 2 1 pointsSave Answer Below are the IR spectrum of aldol on the left and...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • 4. IR SPECTROSCOPY Run the IR spectrum of your product using the Nujol mull technique; attach...

    4. IR SPECTROSCOPY Run the IR spectrum of your product using the Nujol mull technique; attach the spectrum to your report. Cinnamic acid contains a carboxyl group (-CO,H) in which the carbon-oxygen double bond is "conjugated" with the carbon-carbon double bond (C=C-C=O). The C=O stretching absorption appears at about 1685 cm in cinnamic acid. (a) What is the frequency of the CO stretching absorption in your product? (b) What effect does conjugation have on the frequency of the CEO stretching...

  • 4. Analyze the IR spectrum of your product, filling in the table below. You should utilize your c...

    If you could help explain the chart above, that would be awesome. 4. Analyze the IR spectrum of your product, filling in the table below. You should utilize your course textbook (pp. 764-766), if you need assistance. Please note that the frequency given below should be exact (one number), not a range. Use the frequency of the center of the band at its strongest point. Then, on the spectrum itself, mark the characteristic bands at their strongest point with a...

  • Question attached, thanks An IR spectrum was collected for an unknown organic molecule. The spectrum showed...

    Question attached, thanks An IR spectrum was collected for an unknown organic molecule. The spectrum showed several peaks, which have been listed below. Peak 1 = 3039 Peak 2 = 2875 Peak 3 = 1665 Peak 4 = n/a Given this data, which of following was the unknown organic molecule? Please use this table to determine the appropriate ranges for various IR stretches. ondo omoh w Submit Answer Tries 0/2 Bond Type Wavenumber range 2850-2960 C-Halkane 3020-3080 3300 C-Halkene C-Halkyne...

  • i am not sure how to answer the bottom question... Examine the IR spectrum below and...

    i am not sure how to answer the bottom question... Examine the IR spectrum below and identity as molecule (1-chlorohentanel and consider all expe ational modes even in the fingerprint (you do regions of the expected vibrations) entify as many peaks as you can. Draw the structure of the er all expected peaks, labeling them with functional groups serprint (you do not need to label individual peaks, only Heptane, 1-chloro- INFRARED SPECTRUM 800 Iloco Co chloride) c-c. Relative Transmittance Alkane...

  • Chem 210 Report - IR Spectroscopy Name: ID: 1) For the functional group(s) on the following...

    Chem 210 Report - IR Spectroscopy Name: ID: 1) For the functional group(s) on the following molecule what characteristic IR absorption(s) would be expected (ignoring C-H absorptions). A) a peak around 1700 cm–1 B) a peak around 3300 cm–1 C) a peak around 1650 cm–1 D) a peak around 2250 cm–1 E) None of these choices Answer: 2) An oxygen-containing compound shows strong IR absorption at 1630-1780 cm–1 and 3200-3550 –1 cm . What type of compound is it likely...

  • IR of Synthesized Acetaminophen - Use the IR spectrum of your synthesized acetaminophen to answer the...

    IR of Synthesized Acetaminophen - Use the IR spectrum of your synthesized acetaminophen to answer the following questions: 3. Attach an annotated copy of your IR spectrum, with the absorptions corresponding to the stretches from the N-H, O-H, and C-O bonds labeled. (See Collab for an example of an annotated spectrum.) 5 points 4. How, if at all, does your experimental spectrum differ from the spectrum of pure acetaminophen from Collab? List any extra significant peaks and their wavenumber and...

  • IR Spectroscopy of Aspirin 1. Draw the structure of aspirin and state the chemical name of...

    IR Spectroscopy of Aspirin 1. Draw the structure of aspirin and state the chemical name of aspirin. 2. Indicate the regions (circle and label on your IR spectrum) of your spectrum that correspond to a carbonyl and a hydroxyl functional group. Identify two other regions that correlate with other functional groups/structural features. Indicate these regions on your spectrum (circle and label on your IR spectrum). 3. Use your IR spectrum, melting point data, and FeCly test results to characterize the...

  • Questions 2-10 please!! 1) A substitution reaction is: [2] a) A reaction during which an OH...

    Questions 2-10 please!! 1) A substitution reaction is: [2] a) A reaction during which an OH group of a molecule is replaced by a halogen. b) A reaction during which water is the leaving group. c) A reaction during which a functional group of a molecule is replaced by an electrophile. d) A reaction during which a functional group of a molecule is replaced by another functional group. V 12 2) Substitution reactions are classified either as electrophilic or nucleophilic...

  • Please answer the question below, thanks! Problem 10-12A On January 1, 2019, Oriole Company issued $2,780,000...

    Please answer the question below, thanks! Problem 10-12A On January 1, 2019, Oriole Company issued $2,780,000 face value, 12%, 10-year bonds at $2,629,150. This price resulted in an effective-interest rate of 13% on the bonds. Oriole uses the effective-interest method to amortize bond premium or discount. The bonds pay annual interest on January 1. Your answer is correct. Prepare the journal entry to record the issuance of the bonds on January 1, 2019. (Credit account titles are automatically indented when...

  • 1. Signal Assignment. Below are a set of ranges where a specific H' NMR signal might...

    1. Signal Assignment. Below are a set of ranges where a specific H' NMR signal might be found. 0.5-2.0ppm 2.0-3.0ppm 3.0-5.Oppm 0.5-6.Oppm 5.0-7.0ppm 7.0-8.Oppm 9.0-10.0ppm 10.0-12.0ppm Assign to the slots above where the following highlighted protons might be found. a) CH3-CH2- b) CH-CH2-CH2- c) HC-0 d) H-C(O)-R e) H-O-R ) H-O-C(O)-R g) H;C-Ar h ) H-C-C- j) CH3-CEC ...some groups appear in the same ppm range. [2pts each group correctly assigned) 2. Signal Splitting. Decide what splitting pattern (singlet, doublet,...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT