Question

erimental data: a. Calculate the theoretical yield of product from todays experiment. Show your work (1 point) o.sgol = 0.005. IR analysis: a. Label the IR spectrum of trityl chloride with all important functional groups at 1600 cm and higher (1.0 pC. Which peaks in your IR support the formation of product? Which peaks are absent that support the formation of product? FulInfrared Spectrum of Triphenylmethanol w4 40 30. % Transmittance OH. 20 O 10 - 0 4000 3500 3000 2500 10 2000 1500 WavenumbersIR correlation table, from Mohrig, 3rd edition Characteristic infrared absorption peaks of functional groups Vibration Positi

Need help answering questions 5 (a, b, & c), 6, & 7.

Thank you.

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

Ans from melting point data observed 160°C to 163°C which indiccetes melting point is product is formed. 3400 cm to IR IR obsIR spectra 5.ce due to Signal at 1592 cm Aromatic X=(( stretch. Aromatic c.lt Stretch Signal at 3060 cmt due to b of 112 spec

Add a comment
Know the answer?
Add Answer to:
Need help answering questions 5 (a, b, & c), 6, & 7. Thank you. erimental data:...
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
  • 1. Using the IR correlation table on the second image, indicate how you could distanguish between...

    1. Using the IR correlation table on the second image, indicate how you could distanguish between the following pairs of compounds by using infrared spectroscopy. Give two specific absence/appearance of wavrnumbers for each compound: 2. For this experiment, what is the purpose of adding acetone? Predict what would happen if you omitted the acetone in the experimental procedure. 3. Draw four different resonance structures of the triphenylmethyl cation. *IR correlation table PRE-LAB QUESTIONS 1. Using the IR correlation table on...

  • 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...

  • please answer b *PLEASE DO NOT FORGET THE EXPLANATION* b. Circle the most likely structure that...

    please answer b *PLEASE DO NOT FORGET THE EXPLANATION* b. Circle the most likely structure that corresponds to the IR spectrum: Spectrum: Explanation (be specific): Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH -CH2- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne Aldehyde O-H Alcohol, phenols Free H-bonded Carboxylic acids Primary and secondary amines and amides (stretch)...

  • I need help with these questions please! 3. What are the hydrolysis products in the reaction...

    I need help with these questions please! 3. What are the hydrolysis products in the reaction below? Coba 4. Determine if the IR spectrums below belong to benzoic acid or methyl benozate. What are the important types of bonds on each IR spectrum? And what are the bonds frequencies on both IR spectrums? ---------- LAULUDED BELIEU ------------ The IR spectrum for benzaldehyde is below. Identify the bonds that absorb at the following wavenumbers. 3086 cm-1 2860 and 2736 cm-1 1703...

  • please answer C and PLEASE do not forget the explanation C. Circle the most likely structure...

    please answer C and PLEASE do not forget the explanation C. Circle the most likely structure that corresponds to the IR spectrum: OH OH Explanation (be specific): Spectrum: ARVENUHERIA Infrared Absorption Bands Frequency (cm ) Intensity Type of Vibration C-H Alkanes -CH -CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) 3000-2850 1450 and 1375 1465 3100-3000 1000 650 3150 3050 900-690 ca. 3300 2900-2800 2800-2700 Aromatics Alkyne Aldehyde 0-н 3650-3600 3400-3200 3400-2400 Alcohol, phenols Free H-bonded...

  • 3) Four of the compounds below contain carbonyl functional groups. a). What stretching frequency will they...

    3) Four of the compounds below contain carbonyl functional groups. a). What stretching frequency will they have in common? Name the bond and typical cm^-1 b). Are there variations in the stretching frequency that you named above for the different carbonyl functional groups? If so, what?                      Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH --CH, Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690...

  • INFRARED SPECTROSCOPY 1. Circle AND label the functional groups in each molecule. Then predict the signal(s)...

    INFRARED SPECTROSCOPY 1. Circle AND label the functional groups in each molecule. Then predict the signal(s) that would result from each functional group in the IR. PLEASE ANSWER (C) and (D please follow the directions and write neatly Но, ес -CEC-H Infrared Absorption Bands Type of Vibration Frequency (cm21) Intensity C-H Alkanes CH CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne...

  • Please answer the exercise 9.2. I have included the spectrums. Please review attached images and table to help answer questions. Match the compounds to their corresponding spectrums. Thank you very mu...

    Please answer the exercise 9.2. I have included the spectrums. Please review attached images and table to help answer questions. Match the compounds to their corresponding spectrums. Thank you very much! Match each spectrum in exercise 9.2 of your text (pages 449-450) to a compound on the right. Remember that you can use Table 9.2 on page 439 to solve these puzzles along with some of the reading. cycloheptene H2N 4-methylaniline CI p-dichlorobenzene ethynylbenzene 3-methylphenol odobenzene Choose... Exercise 9.2 spectrum...

  • (6 pts)9a. Which of the following compounds is consistent with the following IR spectrum? Clearly show...

    (6 pts)9a. Which of the following compounds is consistent with the following IR spectrum? Clearly show your work to support your choice. Include all signals that discussed in lecture videos. کے NH NHCH NH NH NICHE CH Lo "CHO II IN IV CH, b. Which of the following compounds is consistent with the following IR spectrum? Clearly show your work to support your choice. Include all signals that discussed in lecture videos. m هه wavenumber OH = لہ 'H ځ...

  • 5) Provide a structure consistent with all of the data for the following compounds. Unless otherwise...

    5) Provide a structure consistent with all of the data for the following compounds. Unless otherwise stated, the IR data is not all inclusive, i.e. you may propose a structure which would include peaks not specifically noted but your structure must account for the peaks which are listed or which are excluded. a) Compound Q (C6H100) decolorizes Br2/CC14. IR peaks at 3500 cm- and 1640 cm"! NO absorption between 1700 and 1800 cm? b) Compound K (C6H100) does not decolorize...

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