Reference no: EM131044470
1. Provide the real name (IUPAC name) for each of the following structures.
![280_Figure.png](https://secure.expertsmind.com/CMSImages/280_Figure.png)
2. Label the following as aromatic (A), anti-aromatic (AA) or non-aromatic (NA).
![2340_Figure1.png](https://secure.expertsmind.com/CMSImages/2340_Figure1.png)
3. Assume you are carrying out a reduction reaction of cyclohexanone to give cyclohexanol product as shown below; describe how you will use the following techniques to monitor the reaction:
![89_Figure2.png](https://secure.expertsmind.com/CMSImages/89_Figure2.png)
a. 1H NMR
b. IR
4. From the structure shows below, calculate the multiplicities of proton signals at positions labeled a, b and c.
![1671_Figure3.png](https://secure.expertsmind.com/CMSImages/1671_Figure3.png)
5. Write the number of signals (peaks) expected on (a) 13C NMR and (b) 1H NMR spectra of the following compound.
![586_Figure5.png](https://secure.expertsmind.com/CMSImages/586_Figure5.png)
6. Provide the product (and stereochemistry) for the Diels-Alder reactions.
![2438_Figure6.png](https://secure.expertsmind.com/CMSImages/2438_Figure6.png)
7. Provide the family names of the following compounds.
![501_Figure7.png](https://secure.expertsmind.com/CMSImages/501_Figure7.png)
8. Which will be a stronger acid? Explain why it is stronger.
![1466_Figure8.png](https://secure.expertsmind.com/CMSImages/1466_Figure8.png)
9. Give the fragmentation products of the compounds shown below.
![798_Figure9.png](https://secure.expertsmind.com/CMSImages/798_Figure9.png)
10. The following compounds al show a single line in their 13C NMR spectra. Use numbers 1-4 to label them in their expected order of increasing chemical shifts.
![1049_Figure10.png](https://secure.expertsmind.com/CMSImages/1049_Figure10.png)
11. Provide the product in the following reactions.
![1225_Figure11.png](https://secure.expertsmind.com/CMSImages/1225_Figure11.png)
12. Provide the products for the following reactions.
![1925_Figure12.png](https://secure.expertsmind.com/CMSImages/1925_Figure12.png)
13. Label each statement as "True" or a "False".
- Deshielding results in the chemical shift signal moving further down field.
- Deshielding results in the chemical shift signal moving further up field.
- Deshielding results in the chemical shift signal moving further to the left.
- Deshielding results in the chemical shift signal moving further to the right.
- Deshielding results in the reduction of electron density around the proton nuclei.
- Deshielding results in the increase of electron density around the proton nuclei,
- Homotopic protons have same chemical shift values.
- Enantiotopic protons have same chemical shift values.
- Diastereotopic protons have same chemical shift values.
- Kinetic products are less stable than thermodynamic products.
- Kinetic products are more stable than thermodynamic products.
- Epoxides are also ethers.
- Alcohols are more acidic that carboxylic acids.
- One problem with Friedel-Crafts acylation is the rearrangement of the carbocation intermediate.
- Carboxylate ions are more stable then alkoxide ions.
14. Identify the main functional group present in the spectrum below.
![2263_Figure14.png](https://secure.expertsmind.com/CMSImages/2263_Figure14.png)
15. For the spectrum below, provide the following:
![93_Figure15.png](https://secure.expertsmind.com/CMSImages/93_Figure15.png)
a. M+ ion
b. Base ion
c. Parent peak
d. Molecular peak
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