I have explained in details. Hope this is satisfactory.

how ro label pka and the equivalence point halfway end point 14 C 12 10 2...
Please here is my lab questions for titration of weak acid. The
questions are very short. You have to determine the answers by just
looking at the graph based on the data points. Please give me the
answers of all of them. I would really appreciate. Please calculate
the molar mass question #7 as well. It will be of great help to
me.
Mass of the unknown acid: 0.2grams
Concentration of NaOH = 0.0500M
Formuld Bal pH of weak acid...
Assign label to each hydrogen of vanillyl acetate of NMR
spectrum. Is this correct?
28'6 -9.87 -7.45 -7.18 -3.87 -2.34 Base-catalyzed vanillin esterification product Simulated High Resolution Spectrum 7.45 -7.18 4 TUTM 03 TTTTT 7.7 7.5 7.3 7.1 6.9 Chemical Shift DE A F001 3.06- 3.06- 11.5 10.5 9.5 8.5 7.5 6.5 3.5 2.5 1.5 0.5 -0.5 -1.5 5.5 4.5 Chemical Shift
what is the equivalence point in mL and how do I
calculate it?
FIE LUI E Scale E Print Store Pages Save Open New Run 1 olume HCI (mL) pH 0.5 OWN 4.5 12 5.5 6 12.54 12.51 12.47 12.43 12.39 12.35 12.29 12.24 12.18 12.12 12.04 11.96 11.86 11.74 11.56 11.25 9.95 3.76 2.96 2.73 2.57 2.48 2.41 2.36 6.5 Hd 16 7.5 18 19 8.5 9 20 21 9.5 10 10.5 22 23 11 24 25 11.5 26
I have to complete a lab report for a class using data collected
and I have no idea how to use this data. Please help!
Name Date REPORT SHEET Weak Acid vs. Strong Acid Titration EXPERIMENT 16 Determination of pKa of Unknown Acid Volume at equivalence point: Volume at one half equivalence point: - pka: Ka: Show work below: Concentration of Unknown Weak Acid and HCI Unknown Acid HCl Volume of Acid Molarity of NaOH mL of NaOH at equivalence...
A variety of spectra for an organic compound with molecular
formula C10H16O are presented below. The
experimental accurate mass using (+) APCI source is 153.1280 u. The
1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following
slides. Propose a structure for this unknown and answer or address
the following questions or requirements:
d. If there are still any questionable assignments, propose
additional NMR experiments which would solve those questions and
briefly explain specifically what correlations you...
A variety of spectra for an organic compound with molecular
formula C10H16O are presented below. The
experimental accurate mass using (+) APCI source is 153.1280 u. The
1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following
slides. Propose a structure for this unknown and answer or address
the following questions or requirements:
a. Using the most abundant isotopes of C, H and O, what are the
errors in ppm and milli-Daltons for the experimental accurate
mass?...
analyze this NMR & IR
S23 CDC13 QE-300 240 UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
5. Based on this analysis, the compound might be or contain
the following substructure:
6. How many different types of carbons appear to be present?
What are the chemical shifts for these carbons?
UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
7. What kind of carbons correspond to these chemical
shifts?
8. Based on this analysis, the unknown might contain the
following substructure:
UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
1.
How many different types
of protons appear to be present? What are the chemical shifts for
these protons? What does this indicate (if anything) about the
electronic environment of the protons?
2.
What are the multiplicities for each peak?
UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)