I need help to perdect the ir spectreum digram for the final product   4-Nitrobenzyl Alcohol and also for it need to draw the final product and labled the functional groups on it and on the ir spec digram  I linked an example I made on how it suppose to look, its not the answer just the format

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
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I need help to perdect the ir spectreum digram

for the final product  

4-Nitrobenzyl Alcohol

and also for it need to draw the final product and labled the functional groups on it and on the ir spec digram 

I linked an example I made on how it suppose to look, its not the answer just the format

Experimental Procedure.
You will be using pre-prepared TLC plates and spotters in this experiment.
In a small Erlenmeyer flask, dissolve 200 mg (1.30 mmol) of 4-nitrobenzaldehyde in 10
ml of methanol.
TLC will be used to monitor the progress of your experiment. Prepare a TLC plate so
that two spots will be eluted (Starting material – SM; Crude product 1 – CP1). Spot a
TLC with your starting material (SM). The spot of the 4-nitrobenzaldehyde should be
readily visible by UV, since the compound absorbs very strongly in the UV region.
Take the sodium borohydride out of the dessicator, quickly weigh out 70 mg of NaBH4,
and put the sodium borohydride container back to the dessicator. Add the sodium
borohydride to the Erlenmeyer flask that contains the methanol solution of the 4-
nitrobenzaldehyde, with stirring. In your laboratory notebook, record the time of addition
of sodium borohydride to your reaction flask. Some of the sodium borohydride might not
dissolve in the solution. These particles are an insoluble salt which is a product of the
reaction.
Now spot your second spot (of the reaction mixture that is stirring in your flasks) on the
TLC plate (mark it CP1), and note the time in your lab notebook. While the reaction
mixture is stirring, elute the TLC using 30% ethyl acetate in petroleum ether (30% ethyl
acetate; 70% petroleum ether). Remember to keep the elution solvent below the level of
the TLC spots when you place the plate in the elution chamber.
From this TLC, find out if there is any starting material (4-nitrobenzaldehyde) left in the
reaction mixture. If there is none, stop stirring. Your reduction is complete. If there is still
a spot on the TLC due to the starting material, continue stirring for about five minutes,
then take another TLC with one spot (mark it as CP2). If the reaction is still not complete,
add some more sodium borohydride and continue stirring.
After the reaction has been completed, add about 20 mL of methylene chloride
(dichloromethane/ DCM), and pour the solution into a separatory funnel. Add 20 mL of
water to the separatory funnel. Shake and let the aqueous and organic layers separate.
Place the organic layer (which layer is that?) with your product in an Erlenmeyer flask.
Repeat with another portion of methylene chloride. Combine the organic layers and add a
drying agent. Gravity filter the solution into 100 mL pre-weighed round-bottom flask and
wash the flask and drying agent with an additional 5mL of methylene chloride, also
filtered into your round bottom flask. Evaporate the solvent on a steam bath in the hood
(Erlenmeyer), or use the rotary evaporator (round bottom flask). Weigh the flask again
and calculate the crude yield.
(Be sure all solvent has been removed!)
Transcribed Image Text:Experimental Procedure. You will be using pre-prepared TLC plates and spotters in this experiment. In a small Erlenmeyer flask, dissolve 200 mg (1.30 mmol) of 4-nitrobenzaldehyde in 10 ml of methanol. TLC will be used to monitor the progress of your experiment. Prepare a TLC plate so that two spots will be eluted (Starting material – SM; Crude product 1 – CP1). Spot a TLC with your starting material (SM). The spot of the 4-nitrobenzaldehyde should be readily visible by UV, since the compound absorbs very strongly in the UV region. Take the sodium borohydride out of the dessicator, quickly weigh out 70 mg of NaBH4, and put the sodium borohydride container back to the dessicator. Add the sodium borohydride to the Erlenmeyer flask that contains the methanol solution of the 4- nitrobenzaldehyde, with stirring. In your laboratory notebook, record the time of addition of sodium borohydride to your reaction flask. Some of the sodium borohydride might not dissolve in the solution. These particles are an insoluble salt which is a product of the reaction. Now spot your second spot (of the reaction mixture that is stirring in your flasks) on the TLC plate (mark it CP1), and note the time in your lab notebook. While the reaction mixture is stirring, elute the TLC using 30% ethyl acetate in petroleum ether (30% ethyl acetate; 70% petroleum ether). Remember to keep the elution solvent below the level of the TLC spots when you place the plate in the elution chamber. From this TLC, find out if there is any starting material (4-nitrobenzaldehyde) left in the reaction mixture. If there is none, stop stirring. Your reduction is complete. If there is still a spot on the TLC due to the starting material, continue stirring for about five minutes, then take another TLC with one spot (mark it as CP2). If the reaction is still not complete, add some more sodium borohydride and continue stirring. After the reaction has been completed, add about 20 mL of methylene chloride (dichloromethane/ DCM), and pour the solution into a separatory funnel. Add 20 mL of water to the separatory funnel. Shake and let the aqueous and organic layers separate. Place the organic layer (which layer is that?) with your product in an Erlenmeyer flask. Repeat with another portion of methylene chloride. Combine the organic layers and add a drying agent. Gravity filter the solution into 100 mL pre-weighed round-bottom flask and wash the flask and drying agent with an additional 5mL of methylene chloride, also filtered into your round bottom flask. Evaporate the solvent on a steam bath in the hood (Erlenmeyer), or use the rotary evaporator (round bottom flask). Weigh the flask again and calculate the crude yield. (Be sure all solvent has been removed!)
Grouplwaven Fndtioral Group
a
sp EH stretch
Benzene
sp?-c-H stretch
H
benren
C 1600
sp3 (-H
Stretch
sp2 C-H
stretch
HIJ- =
it
Transcribed Image Text:Grouplwaven Fndtioral Group a sp EH stretch Benzene sp?-c-H stretch H benren C 1600 sp3 (-H Stretch sp2 C-H stretch HIJ- = it
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