1. Look online to find the IR spectrum of cis-norbornene-5,6-endo-dicarboxylic anhydride: what do the signals at 1759 cm-1 and 1838 cm-1 indicate?
1. Look online to find the IR spectrum of cis-norbornene-5,6-endo-dicarboxylic anhydride: what do the signals at...
Examine the IR spectrum of cis-norbornene-5,6-endo-dicarboxylic anhydride, (Fig.48.8, pp. 630): what do the signals at 1750 cm-1 and 1838 cm-1 indicate?
1.
Examine the IR spectrum of cis-norbornene-5,6-endo-dicarboxylic
anhydride, (Fig.48.8, pp. 630): what do the signals at 1750 cm-1
and 1838 cm-1 indicate?
2. Explain the following questions regarding the possible
contamination of the final isolated product with dicyclopentadiene
(the cyclopentadiene dimer).
a. Since “cracked” cyclopentadiene can spontaneously dimerize
back to dicyclopentadiene, could the dimer be formed as an unwanted
“by-product” during the experiment?
b. How does the experimental procedure minimize contamination of
the final isolated (desired) product with this (undesired)...
1. Examine the IR spectrum of cis-norbornene-5,6-endo-dicarboxylic anhydride, (Fig.48.8, pp. 630): (this is out of macroscale and microscale organic experiments 6e textbook can be googled to view) what do the signals at 1750 cm-1 and 1838 cm-1 indicate? (please include functional groups, structures, as much as possible so i can understand it) Thank you!
How would I calculate the theoretical yield of
endo-cis-norbornene-5,6-endo-dicarboxylic anhydride and
endo-cis-norbornene-5,6-dicarboxylic acid? Can you please show me
step by step? Can you show me the balanced chemical equation (with
molecular formulas, not the pictures) with the mole ratios as well?
How do we figure out the limiting reagent? Can you also show how to
convert mL to grams for cyclopentadiene, if needed?
We used:
2g of maleic acid
6mL of ethyl acetate
6mL of ligroin (hexanes)
2mL of cyclopentadiene...
Provide a full mechanism of the preparation of
Endo-norbornene-cis-5,6-dicarboxylic acid with
dicylclopentadiene and maleic anhydride
| СОН НОС
Endo-norbornene-cis-5,6-dicarboxylic acid can be converted back into its anhydride precursor by treatment with anhydrous acid. Propose a mechanism for this reaction.
Reaction 0 Maleic anhydride mp 53°C, MW 98.06 cis-Norbornene-5,6-endo-dicarboxylic anhydride mp 165°C, MW 164.16 Problem: 1) You are given 1 mL of freshly distilled cyclopentadiene in a clean vial and I g of maleic anhydride in weigh boat. The mass of the final product is 1.1g. A) Calculate percent yield. B) Interpret IR spectrum of product (shown below) and provide a table listing functional groups and peak intensity, 5. Which of the following dienes are s-trans and which are s-cis?...
provide a mechanistic description (with arrows) for all
reactions in the above preparation of
endo-norbornene-cis-5,6-dicarboxylic acid.
1) оо 2) Но СОН НОС
penauere more reactive Wire any chiral centers does endo-norbornene-cis-5,6-dicarboxylic acid possess? Is the molecule itself chiral? (continued) 51
5. (a) compare the carbonyl region of your IR spectrum with
that of maleic anhydride. What are the similarities? what are the
differences?
(b) Does your IR spectrum allow you to confirm that the
structure of the product is a combination of the two reactants?
Briefly explain.
%Transmittance 4000 & & 8 8 8 8 8 8 98 dies alder product... 3500 3000 3077.17 2980 22 2970.61 2322 69 2500 Wavenumbers (cm-1) 2000 2168.29 1701,39 1861.48 1843.97 1808.95 1780.00 1654.10...