For each peak of the NMR, describe the chemical shift, functional group, integration, splitting pattern, neighbors,...
Part 2: Draw the NMR spectrum: Draw the structure of your molecule below, indicating each unique hydrogen atom with letters, starting with A. After complete the below table, summarizing the integration, approximate chemical shift, number of neighbors, and splitting pattern of each hydrogen in your given molecule. Note, you do not need to fill every row in the below table. By CH₃ Structures H₂C- 2 Brono- 4 methyl pertane Hydrogen Integration Letter A Chemical Number of Splitting Pattern Shift Neighbors...
n-Butanol ОН Part 2: Draw the NMR spectrum Draw the structure of your molecule below, indicating each unique hydrogen atom with letters, starting with A. After complete the below table, summarizing the integration, approximate chemical shift number of neighbors, and splitting pattern of each hydrogen in your given molecule. Note, you do not need to fill every row in the below table. Structure: Hydrogen Integration Letter Chemical Number of Splitting Pattern Shift Neighbors Now, draw the NMR in the space...
predict the 1H NMR Spectra with the molecule. include the integration, chemical shift and splitting pattern H. H₃ C' chemical formula : ciotoo
predict the 1H NMR Spectra with the molecule. include the integration, chemical shift and splitting pattern Осм3 Нас. TZ Оснэ chemical formua: C14H21N03
1H NMR SPECTRA no.13 STUDENT NAME (1) Cult;$O Diwwer Number Chemical Shift Splitting pattern Integration which protons Structure
Draw the expected H NMR spectrum for each molecule. Pay attention to the chemical shift and splitting. Mark the integration of each peak. Then assign each peak in the NMR to hydrogen atoms in the structure. HyC 0 ppm 192 t2 .3 +5 o t6 O=C +7 C=O +8
provide a summary of the peaks in the H NMR spectra of your solid unkown. for each peak, note the approximate chemical shift, splitting pattern, and intergration do do
formula is C4H10O 1. Fill in the table below. (7 pts.) Peak letter Chemical shift Splitting pattern Integration # Type of H that made the peak (i.e CH) 2. Calculate the degree of unsaturation for your compound. (3 pts.) 3. Predict a structure for your unknown compound. (5 pts.) 4. Label the hydrogens in your structure with the letter of the NMR peak with which they correspond. (5pts.) 5. Explain how you arrived at your predicted structure. For example, "The...
Draw the structures of each and predict the 1H NMR spectrum (approximate chemical shift, integration and splitting): a) anisole b) 4-nitrotoluene
Liquid Extraction NMR and IR The 'H NMR for the unknown C: 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm Proton peak Integration Neighbors (n) Chemical Shift (ppm) Splitting pattern (n+1) (report as singlet/doublet/triplet/ete. 9 b. C must be an aliphatic alcohol. There is a strong O-H stretch in the IR and zero degrees of unsaturation. The remaining structure is determined by 'H NMR. (c) Predicted Structure C (label hydrogens with...