Chapter 17: Q.3. (page 641)
Question: Give the IUPAC name for each compound.
a.
b.
c.
d.
Short Answer
Answer
- m-1,3-diisopropylbenzene
- 1-sec-butyl-4-ethylbenzene
- m-butylphenol
- 2-bromo-5-chlorotoulene
Chapter 17: Q.3. (page 641)
Question: Give the IUPAC name for each compound.
a.
b.
c.
d.
Answer
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Get started for freeQuestion: Explain why triphenylene resembles benzene in that it does not undergo addition reactions with , but phenanthrene reacts with to yield the addition product drawn. (Hint: Draw resonance structures for both triphenylene and phenanthrene, and use them to determine how delocalized each bond is.)
Question: Answer the following questions about curcumin, a yellow pigment isolated from turmeric, a tropical perennial in the ginger family and a principal ingredient in curry powder.
a. In Chapter 11 we learned that most enols, compounds that contain a hydroxy group bonded to a C=C, are unstable and tautomerize to carbonyl groups. Draw the keto form of the enol of curcumin, and explain why the enol is more stable than many other enols.
b. Explain why the enol O-H proton is more acidic than an alcohol O-H proton.
c. Why is curcumin colored?
d. Explain why curcumin is an antioxidant.
Draw the structure corresponding to each name
Question: What is the structure of propofol, which has the IUPAC name 2,6-diisopropylphenol? Propofol is an intravenous medication used to induce and maintain anesthesia.
Question: Draw all aromatic hydrocarbons that have molecular formula . For each compound, determine how many isomers of molecular formula would be formed if one H atom on the benzene ring were replaced by a Br atom.
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