Principles of Modern Chemistry
8th Edition
ISBN: 9781305079113
Author: David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Publisher: Cengage Learning
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Chapter 7, Problem 4P
A gaseous
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Aldehydes and ketones can be named in a systematic way by counting the number of carbon atoms (including the carbonyl carbon) that they contain. The name of the aldehyde or ketone is based on the hydrocarbon with the same number of carbon atoms. The ending -al for aldehyde or -one for ketone is added as appropriate. Draw the structural formulas for 3-methyl-2-butanone.
Indicate whether each statement is true or false.
Pentane has higher molar mass than hexane.
The longer the linear alkyl chain for straight-chain hydrocarbons, the higher the boiling point.
The local geometry around the alkyne group is linear.
Propane has two structural isomers.
Determine the mass of 2-bromopropane that could be prepared from 25.5 g of propene? assume a 100% yield of the product?
Chapter 7 Solutions
Principles of Modern Chemistry
Ch. 7 - Prob. 1PCh. 7 - Is it possible for a motor fuel to have a negative...Ch. 7 - A gaseous alkane is burned completely in oxygen....Ch. 7 - A gaseous alkyne is burned completely in oxygen....Ch. 7 - Write a chemical equation involving structural...Ch. 7 - Prob. 6PCh. 7 - Prob. 7PCh. 7 - Prob. 8PCh. 7 - Prob. 9PCh. 7 - Prob. 10P
Ch. 7 - Prob. 11PCh. 7 - Prob. 12PCh. 7 - Prob. 13PCh. 7 - State the hybridization of each of the carbon...Ch. 7 - Prob. 15PCh. 7 - Prob. 16PCh. 7 - Prob. 17PCh. 7 - In a recent year, the United States produced...Ch. 7 - Prob. 19PCh. 7 - Prob. 20PCh. 7 - Prob. 21PCh. 7 - Prob. 22PCh. 7 - Prob. 23PCh. 7 - Prob. 24PCh. 7 - Prob. 25PCh. 7 - Prob. 26PCh. 7 - Acetic acid can be made by the oxidation of...Ch. 7 - Acrylic fibers are polymers made from a starting...Ch. 7 - Compare the bonding in formic acid (HCOOH) with...Ch. 7 - Prob. 30PCh. 7 - Prob. 31PCh. 7 - Prob. 32PCh. 7 - Prob. 33PCh. 7 - Prob. 34PCh. 7 - Prob. 35PCh. 7 - Describe the changes in hydrocarbon structure and...Ch. 7 - trans-Cyclodecene boils at 193C, but...Ch. 7 - Prob. 38APCh. 7 - Prob. 39APCh. 7 - Consider the following proposed structures for...Ch. 7 - Prob. 41APCh. 7 - Prob. 42APCh. 7 - Prob. 43APCh. 7 - Prob. 44APCh. 7 - Prob. 45APCh. 7 - The steroid stanolone is an androgenic steroid (a...Ch. 7 - The structure of the molecule cyclohexene is Does...Ch. 7 - Prob. 48CP
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- What is the difference in bonding and in the general molecular formula between an alkene and an alkane with the same number of carbon atoms?arrow_forward1. Which of the following formulas is incorrect?a. CaNO3b. MgSc. AlBr3d. Li2Oe. NaOH 2. Part of an organic molecule where most of its chemical reactions occur.a. Substrateb. Productc. Reactantsd. Functional Group 3. An acyclic unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds. As the family name alkyne indicates the characteristics ending associated with a triple bond. It has a general formula of one triple bond is CnH2n-2.a. Alkenesb. Alkynesc. Aromatic compoundd. Cycloalkanearrow_forwardComplete the following reactions for alkynes. Draw the structure of the product. Name the reactant and the product.arrow_forward
- State whether the statements are true or false. 1. Unsaturated hydrocarbons must contain at least one carbon-carbon double triple bond. 2. Aromatic compounds usualky undergo addition reactions. 3. Carboxylic acid molecules are much less polar than the corresponding alkane molecules. 4. Marikovnikov's rule states that, in an addition reaction involving a hydrogen atom, the hydrogen atom will usually bond to the carbon atom with the fewest hydrogen atoms attached. 5. But-1-ene and 2-ene are structural isomers of each other. 6. Aldehydes contain a carbonyl group on the terminal carbon atom.arrow_forwardHalogenoalkanes undergo two different types of reaction, substitution and elimination reactions depending on the conditions. Use the reaction between 2-bromopropane and sodium hydroxide to explain the chemical reactions of haloalkanes. You must include the following in your explanation: Describe what change is taking place to the halogenoalkane and the product(s) formed. The reaction equations The conditions under which the reactions occur.arrow_forwardSynthesis of benzene compounds. Write the product of the reactions.arrow_forward
- Halogenoalkanes undergo two different types of reaction, substitution and elimination reactions depending on the conditions. Use the reaction between 2-bromopropane and sodium hydroxide to explain the chemical reactions of haloalkanes. You must include the following in your explanation: Describe what change is taking place to the halogenoalkane and the product(s) formed. The reaction equations The conditions under which the reactions occur. please provide a written explain as wellarrow_forwardName and write the structures of all isomers of the propyl and butyl alkyl groups.arrow_forwardAldehydes and ketones can be named in a systematic way by counting the number of carbon atoms (including the carbonyl carbon) that they contain. The name of the aldehyde or ketone is based on the hydrocarbon with the same number of carbon atoms. The ending -al for aldehyde or -one for ketone is added as appropriate. Draw the structural formulas for propanal.arrow_forward
- Explain oxidation and reduction with respect to organic compounds. Give an examplearrow_forward1. Most margarines have been hydrogenated to maintain a soft, homogeneous mixture. While the product is easy to spread, this has made the product an unhealthy choice. A hydrogenation reaction is used to convert an alkene to an alkane. a carboxylic acid to an aldehyde. an alkene to a ketone an aromatic hydrocarbon to a linear hydrocarbonarrow_forwardMark the correct statements about the structural features of alkenes and alkynes. * A- Free rotation is not possible around a double or triple bond. B- A triple bond is shorter and stronger than a double bond. C- A pi-bond can only form by overlap of p-orbitals on adjacent atoms if these atoms are from the same element. D- The pi-bond in an alkene is weaker than the sigma bond because the sideways overlap of p-orbitals is less than the head-to-head overlap of sp² hybrid orbitals. E- All the bond angles in an alkyne are 180°.arrow_forward
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