You have reacted acetic anhydride with an alcohol in the presence of a small amount of concentrated sulfuric acid inthe hope of generating butyl acetate. After isolation by extraction, you subject a small amount of the isolated materialto infra-red analysis. Which of the following may indicate a successful reaction?A sharp peak at 1735 cm , along with other sharp peaks around 2980, 2950 and 2890 cm1A sharp peak at 1700 cm-1, along with a broad peak between 3200 and 2650 cm1Two sharp peaks at 1780 and 1840 cm', along with sharp peaks at 2980, 2950 and 2880 cmA broad peak at 3600 cm, along with sharp peaks at 2980, 2950 and 2880 cm

Note : n-butanaol react with acetic anhydride and acid gives n-butyl acetate. 1735 cm-1 carbonyl…

You have reacted acetic anhydride with an alcohol in the presence of a small amount of concentrated sulfuric acid in the hope of generating butyl acetate. After isolation by extraction, you subject a small amount of the isolated material to infra-red analysis. Which of the following may indicate a successful reaction? O A sharp peak at 1735 cm, along with other sharp peaks around 2980, 2950 and 2890 cm1 OA sharp peak at 1700 cm-1, along with a broad peak between 3200 and 2650 cm1 Two sharp peaks at 1780 and 1840 cm, along with sharp peaks at 2980, 2950 and 2880 cm A broad peak at 3600 cm, along with sharp peaks at 2980, 2950 and 2880 cm

You have reacted acetic anhydride with an alcohol in the presence of a small amount of concentrated sulfuric acid in the hope of generating butyl acetate. After isolation by extraction, you subject a small amount of the isolated material to infra-red analysis. Which of the following may indicate a successful reaction? O A sharp peak at 1735 cm, along with other sharp peaks around 2980, 2950 and 2890 cm1 OA sharp peak at 1700 cm-1, along with a broad peak between 3200 and 2650 cm1 Two sharp peaks at 1780 and 1840 cm, along with sharp peaks at 2980, 2950 and 2880 cm A broad peak at 3600 cm, along with sharp peaks at 2980, 2950 and 2880 cm

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...

See similar textbooks

Similar questions

A student performed a reaction using 2-methoxyethanol as solvent under acid catalyst. When the solvent was redistilled, a higher boiling fraction (bp=162 °C) was also recovered. The mass spectrum showed a molecular ion at 134 m/z. The H nmr spectrum showed a triplet integrating for 2 at 3.55 ppm, a second triplet integrating for 2 at 3.65 ppm, and a singlet integrating for 3 at 3.4 ppm. Give the structure of the newly formed material that is consistent with this data.
can u please explain ur answers thank u
Determine the structure of the unknown compound using the following information. Please show what information are deduced for each spectra which can help predict the structure. From IR Spectra: See the attached picture. From Mass Spectra M+ = 162 base peak = 147 peaks at 43 and 91 From Proton and Carbon NMR Spectra See attached picture.
Interpret the 1H NMR spectrum of Indole-3-Carboxaldehyde
Can you please help me analyze these spectrum tests. The spectrum tests used were FTIR and 1H-NMR. the experiment is ester hydrolysis and 1,7-Dimethyl-heptanedioate, diethyl ether, KOH, and HCl were used.
Analyse the spectra and write the name of the compound. Also write brief explanation for each spectra verifying the parts of your suggested molecule (For IR indicate the functional groups which matches the peaks, for mass indicate the fragments, for CNMR and HNMR indicate which peak belongs to what).
i will upvote plz in detail
Determine which of the following belongs to this ir spectra then complete the nmr analysismethyl butanoate benzaldehyde 1-chlorobutane 1-chloro-2-methylpropane butan-2-one propan-2-ol propanal
Give the structure that corresponds to the following molecular formula and'H NMR spectrum: This compound undergoes catalytic hydrogenation to give 2,2,4-trimethylpentane. chemical shift, Hz 2400 2100 1800 1500 1200 900 600 300 0.89 Hz 8100 C3H16 1.4 Hz 0.89 Hz 1750 2612, 875 865 8. .5 4 1 chemical shift, ppm (8) The magenta numbers in the spectrum are the relative integrals in arbitrary units, and the violet numbers are coupling constants. Draw the compound. Select Draw Rings More Erase H. 6 C.
Following are the IR, MS(EI), 1 H and 13C NMR for an unknown compound. a) Provide the structural formula for the unknown compound. b) Explain the IR, 1 H NMR and MS(EI) spectra based on the structure given in (a).
How do you draw the reaction scheme for this?
analyse the spectra and write the name of the compound. Also write brief explanation for each spectra verifying the part of you suggested molecule (For IR indicate the functional groups which matches the peaks, for mass indicate the fragments, for CNMR and HNMR indicate which peak to what).(maximum character: 60000)