4. Draw the 'H-NMR for the structure below. Label each peak on the NMR (2 points):
2. Draw the 'H-NMR for the structure below. Label each peak on the NMR (2 points):
Can anyone help with this?
2. Draw the 'H-NMR for the structure below. Label each peak on the NMR (2 points):
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...
PLEASE CLEARLY
LABEL EACH PEAK ON THE COMPOUND STRUCTURE AND CORRESPONDING PEAK AS
A), B), C).... ON EACH GRAPH
- Write the Structural formula above both the H-NMR and C-NMR
spectra
- Assign each NMR peak as a), b), c), ... on both your
structural formula and corresponding peaks
- Assign the H-NMR splitting pattern multiplicity for each set
of peaks
BU T LER IO CCHIO baya I C-13 NMA TTTTTTTTTTTTTTTTTT 20 10 PPM
1. Provide the products for the following reactions (1 points). NaOH, Ethanol 2. Draw the mechanism for the reaction above (2 points). 3. Draw the 1H-NMR for the structure below. Label each peak on the NMR (2 points): DE H CE
1. Provide the structure of the compound illustrated in the
below H-NMR spectrum. Label the sets of unequivalent hydrogens in
your structure. The formula for the structure is
C6H10O2.
2. What is the complex splitting pattern for He?
3. Draw the complex splitting pattern for He and
label the coupling constants (J).
4. Why is He more downfield than He?
Include drawings to support your answer.
1н 1H 2H ЗН Зн PPM
Predict the splitting patterns for each peak in the 'H NMR spectrum for the compounds below. Use multiplicity terms such as simples de Net (d) tripler(t). uarter (9) maripler (m), etc. and lahe the corresponding atoms on sach structure accordingly. 4. The compound that gives the following NMR spectrum has the molecular formula CH.B. Draw the structure. CyHxBry 4.00 197 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 24 23 22 21 20
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...
Label each peak clearly and match up with each type of H on
the 1H-NMR. In the IR spectrum label the functional groups.
Write one paragraph to show your reasoning for choosing the
structure. Elaborate on characteristic peaks, patterns and
splitting of signals.
Stay well and healthy! Hold on!
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QUESTIONS 1. NMR (2 Points) Draw the structure of acetaminophen and label chemically-equivalent hydrogen atoms with the same lowercase letter. a. b. (2 Points) Find the peaks that represent these protons on the NMR spectrum of Tylenol, and write down the chemical shift of those peaks next to the protons you labeled nu differences in the peaks in the Excedrin and Tylenol