Chapter 22: Problem 126
Use shorthand line notation (see Exercise 125\()\) to illustrate the structural isomers of \(\mathrm{C}_{7} \mathrm{H}_{16}\) .
Chapter 22: Problem 126
Use shorthand line notation (see Exercise 125\()\) to illustrate the structural isomers of \(\mathrm{C}_{7} \mathrm{H}_{16}\) .
All the tools & learning materials you need for study success - in one app.
Get started for freeDraw the following. a. cis-2-hexene b. trans-2-butene c. cis-2,3-dichloro-2-pentene
Alcohols are very useful starting materials for the production of many different compounds. The following conversions, starting with 1-butanol, can be carried out in two or more steps. Show the steps (reactants/catalysts) you would follow to carry out the conversions, drawing the formula for the organic product in each step. For each step, a major product must be produced. (See Exercise \(68 . )\) (Hint: In the presence of \(\mathrm{H}^{+},\) an alcohol is converted into an alkene and water. This is the exact reverse of the reaction of adding water to an alkene to form an alcohol.) $$ \begin{array}{l}{\text { a. } 1 \text { -butanol } \longrightarrow \text { butane }} \\ {\text { b. } 1 \text { -butanol } \longrightarrow 2 \text { -butanone }}\end{array} $$
Helicenes are extended fused polyaromatic hydrocarbons that have a helical or screw-shaped structure. a. A \(0.1450-\) g sample of solid helicene is combusted in air to give 0.5063 \(\mathrm{g} \mathrm{CO}_{2}\) . What is the empirical formula of this helicene? b. If a 0.0938 -g sample of this helicene is dissolved in 12.5 g of solvent to give a 0.0175 M solution, what is the molecular formula of this helicene? c. What is the balanced reaction for the combustion of this helicene?
For each of the following alcohols, give the systematic name and specify whether the alcohol is primary, secondary, or tertiary
If one hydrogen in a hydrocarbon is replaced by a halogen atom, the number of isomers that exist for the substituted compound depends on the number of types of hydrogen in the original hydrocarbon. Thus there is only one form of chloroethane (all hydrogens in ethane are equivalent), but there are two isomers of propane that arise from the substitution of a methyl hydrogen or a methylene hydrogen. How many isomers can be obtained when one hydrogen in each of the compounds named below is replaced by a chlorine atom? $$ \begin{array}{ll}{\text { a. } n \text { -pentane }} & {\text { c. } 2,4 \text { -dimethylpentane }} \\ {\text { b. } 2 \text { -methylbutane }} & {\text { d. methylcyclobutane }}\end{array} $$
What do you think about this solution?
We value your feedback to improve our textbook solutions.