Chapter 21: Problem 33
There is only one compound that is named 1,2 -dichloroethane, but there are two distinct compounds that can be named 1,2-dichloroethene. Why?
Chapter 21: Problem 33
There is only one compound that is named 1,2 -dichloroethane, but there are two distinct compounds that can be named 1,2-dichloroethene. Why?
All the tools & learning materials you need for study success - in one app.
Get started for freeMarathon Problems. These problems are designed to incorporate several concepts and techniques into one situation. For each of the following, fill in the blank with the correct response. All of these fill-in-the-blank problems pertain to material covered in the sections on alkanes, alkenes and alkynes, aromatic hydrocarbons, and hydrocarbon derivatives. a. The first "organic" compound to be synthesized in the laboratory, rather than being isolated from nature, was _____________which was prepared from____________. b. An organic compound whose carbon-carbon bonds are all single bonds is said to be______. c. The general orientation of the four pairs of electrons around the carbon atoms in alkanes is_______. d. Alkanes in which the carbon atoms form a single unbranched chain are said to be_______alkanes. e. Structural isomerism occurs when two molecules have the same number of each type of atom but exhibit different arrangements of the_______between those atoms. f. The systematic names of all saturated hydrocarbons have the ending_______ added to a root name that indicates the number of carbon atoms in the molecule. g. For a branched hydrocarbon, the root name for the hydrocarbon comes from the number of carbon atoms in the _________continuous chain in the molecule. h. The positions of substituents along the hydrocarbon framework of a molecule are indicated by the ________of the carbon atom to which the substituents are attached. i. The major use of alkanes has been in_______reactions,as a source of heat and light. J. With very reactive agents, such as the halogen elements, alkanes undergo _______reactions, whereby a new atom replaces one or more hydrogen atoms of the alkane. k. Alkenes and alkynes are characterized by their ability to undergo rapid, complete ______ reactions, by which other atoms attach themselves to the carbon atoms of the double or triple bond. 1\. Unsaturated fats may be converted to saturated fats by the process of ________ m. Benzene is the parent member of the group of hydrocarbons called ________ hydrocarbons. n. An atom or group of atoms that imparts new and characteristic properties to an organic molecule is called a ___________ group. 0.4 _________alcohol is one in which there is only one hydrocarbon group attached to the carbon atom holding the hydroxyl group. p. The simplest alcohol, methanol, is prepared industrially by the hydrogenation of ________ q. Ethanol is commonly prepared by the __________of certain sugars by yeast. r. Both aldehydes and ketones contain the _______group but they differ in where this group occurs along the hydrocarbon chain. s. Aldehydes and ketones can be prepared by _______ of the corresponding alcohol. t. Organic acids, which contain the __________ group, are typically weak acids. u. The typically sweet-smelling compounds called ____________ result from the condensation reaction of an organic acid with an___________.
Oxidation of an aldehyde yields a carboxylic acid: Draw the structures for the products of the following oxidation reactions. a. propanal \(\stackrel{\text { [ox] }}{\rightarrow}\) b. 2,3 -dimethylpentanal \(\stackrel{\text { [ox] }}{\longrightarrow}\) c. 3 -ethylbenzaldehyde \(\stackrel{\text { [ox] }}{\longrightarrow}\)
A confused student was doing an isomer problem and listed the following six names as different structural isomers of \(\mathbf{C}_{7} \mathbf{H}_{16}.\) a. \(1-\) sec-butylpropane d. 1 -ethyl- 1 -methylbutane b. 4 -methylhexane e. 3 -methylhexane c. 2 -ethylpentane f. 4 -ethylpentane How many different structural isomers are actually present in these six names?
A compound containing only carbon and hydrogen is \(85.63 \%\) C by mass. Reaction of this compound with \(\mathrm{H}_{2} \mathrm{O}\) produces a secondary alcohol as the major product and a primary alcohol as the minor product. (See Exercise 62.) If the molar mass of the hydrocarbon is between 50 and 60 g/mol, name the compound.
What is polystyrene? The following processes result in a stronger polystyrene polymer. Explain why in each case. a. addition of catalyst to form syndiotactic polystyrene b. addition of 1,3 -butadiene and sulfur c. producing long chains of polystyrene d. addition of a catalyst to make linear polystyrene
What do you think about this solution?
We value your feedback to improve our textbook solutions.