Concept explainers
(a)
Interpretation:
The structure for the given IUPAC name is to be drawn.
Concept introduction:
An
(b)
Interpretation:
The structure for the given IUPAC name is to be drawn.
Concept introduction:
An alkane is said to be substituted if a hydrogen atom of the alkane is replaced by another atom or group of atoms. In the IUPAC name of a molecule, the root defines the number of carbon atoms in the longest chain. The names of the substituents and their respective locant numbers show the carbon atoms of the root to which the substituents are attached.
(c)
Interpretation:
The structure for the given IUPAC name is to be drawn.
Concept introduction:
An alkane is said to be substituted if a hydrogen atom of the alkane is replaced by another atom or group of atoms. In the IUPAC name of a molecule, the root defines the number of carbon atoms in the longest chain. The names of the substituents and their respective locant numbers show the carbon atoms of the root to which the substituents are attached.
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Chapter A Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction.(Use condensed structural formula) (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene(c) Reaction of (4E)-2,4-Dimethylhexa-1,4-diene with a mole of waterarrow_forward(a) What structural feature is associated with each type of hydrocarbon: alkane, cycloalkane, alkene, and alkyne?(b) Give the general formula for each type.(c) Which hydrocarbons are considered saturated?arrow_forwardDraw line structures for the following alkenes. Which can exist as cis–trans isomers? For those that can, draw both isomers.(a) 2-Methyloct-2-ene (b) Hept-3-ene(c) 3,4-Dimethylhex-3-enearrow_forward
- Draw the product resulting from mild oxidation of (a) 2-butanol; (b) 2-methylpropanal; (c) cyclopentanol.arrow_forwardDraw condensed formulas for the following compounds:(a) 3-ethyl-3-methyloctane; (b) 1-ethyl-3-propylcyclohexane (also draw a carbon-skeleton formula for this compound); (c) 3,3-diethyl-1-hexyne; (d) trans-3-methyl-3-heptene.arrow_forwardA certain hydrocarbon has a molecular formula of C5H8. Which of the following is not a structural possibility for this hydrocarbon? (a) It is a cycloalkane. (b) It contains one ring and one double bond. (c) It contains two double bonds and no rings. (d) It is an alkyne.arrow_forward
- Given each of the IUPAC names provided, draw the corresponding structure. (a) 1-cyclopentylhexane;(b) cyclohexylcyclohexane; (c) 1,2-dicyclopropylnonanearrow_forwardDraw structures for the following molecules. (a) 2-iodo-2,3-dimethylheptane (b) 4-cyclopropyl-3-ethyl-2-methyloctane (c) 1-ethyl-2,4-dimethylcyclopentanearrow_forwardGive the structural formulae and name the functional groups of the following compounds. (a) 3-chlorobut-1-ene Name the functional group: (b) butanedioic acid Name the functional group: (c) propanamide Name the functional group: (d) 3-methylbutanal Name the functional group:arrow_forward
- Indicate whether each statement is true or false. (a) Alkanesdo not contain any carbon–carbon multiple bonds.(b) Cyclobutane contains a four-membered ring. (c) Alkenescontain carbon–carbon triple bonds. (d) Alkynes containcarbon–carbon double bonds. (e) Pentane is a saturatedhydrocarbon but 1-pentene is an unsaturated hydrocarbon.(f) Cyclohexane is an aromatic hydrocarbon. (g) The methylgroup contains one less hydrogen atom than methane.arrow_forward5. Give the structural formulae and name the functional groups of the following compounds. (a) 3-chlorobut-1-ene (b) butanedioic acid Name the functional group: (c) propanamide Name the functional group: (d) 3-methylbutanal Name the functional group: Name the functional group:arrow_forward(B) Draw a structural diagram for each of the following organic compounds: (a) 2-ethyl-4-methyl-2-pentanol (b) 1,2-ethandiol (c) 1,3-dimethylbenzenearrow_forward
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning