Chapter 22: Problem 1
Why can carbon form so many different compounds?
Short Answer
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Chapter 22: Problem 1
Why can carbon form so many different compounds?
These are the key concepts you need to understand to accurately answer the question.
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Get started for freeGive the structure of each of the following aromatic hydrocarbons. $$ \begin{array}{ll}{\text { a. } o \text { -ethyltoluene }} & {\text { c. } m \text { -diethylbenzene }} \\ {\text { b. } p \text { -di-tert-butylbenzene }} & {\text { d. } 1 \text { -phenyl-2-butene }}\end{array} $$
Esterification reactions are carried out in the presence of a strong acid such as \(\mathrm{H}_{2} \mathrm{SO}_{4} \cdot \mathrm{A}\) carboxylic acid is warmed with an alcohol, and an ester and water are formed. You may have made a fruity-smelling ester in the lab when studying organic functional groups. Name the carboxylic acid that is necessary to complete the following esterification reaction.
ABS plastic is a tough, hard plastic used in applications requiring shock resistance. The polymer consists of three monomer units: acrylonitrile \(\left(\mathrm{C}_{3} \mathrm{H}_{3} \mathrm{N}\right),\) butadiene \(\left(\mathrm{C}_{4} \mathrm{H}_{6}\right),\) and styrene \(\left(\mathrm{C}_{8} \mathrm{H}_{8}\right)\) a. Draw two repeating units of ABS plastic assuming that the three monomer units react in a \(1 : 1 : 1\) mole ratio and react in the same order as the monomers listed above. b. A sample of ABS plastic contains 8.80\(\% \mathrm{N}\) by mass. It took 0.605 \(\mathrm{g} \mathrm{Br}_{2}\) to react completely with a 1.20 -g sample of \(\mathrm{ABS}\) plastic. What is the percent by mass of acrylonitrile, butadiene, and styrene in this polymer sample? c. ABS plastic does not react in a \(1 : 1 : 1\) mole ratio among the three monomer units. Using the results from part b, determine the relative numbers of the monomer units in this sample of ABS plastic.
In the presence of light, chlorine can substitute for one (or more) of the hydrogens in an alkane. For the following reactions, draw the possible monochlorination products. $$ 2,2 \text { -dimethylpropane }+\mathrm{Cl}_{2} \longrightarrow $$ $$ 1,3 \text { -dimethylcyclobutane }+\mathrm{Cl}_{2} \stackrel{\mathrm{hn}}{\longrightarrow} $$ $$ 2,3 \text { -dimethylbutane }+\mathrm{Cl}_{2} \stackrel{\mathrm{w}}{\longrightarrow} $$
In general terms, what does the tertiary structure of a protein represent? Distinguish between the secondary and tertiary structures of a protein.
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