(a)
Interpretation:
The systematic name of the compound
Concept Introduction:
Rules for naming compound:
- 1) The carbon atoms in the longest chain have to be counted.
- 2) The substituents and multiple bonds have to be identified and counted and the suffix “-ene” is added.
- 3) The backbone carbon atoms have to be numbered by assigning the lowest number from the starting end that contains the double bond.
Rules for naming compound:
- 1) The carbon atoms in the longest chain have to be counted.
- 2) The substituents and multiple bonds have to be identified and counted and the suffix “-yne” is added.
- 3) The backbone carbon atoms have to be numbered by assigning the lowest number from the starting end that contains the double bond.
Geometrical isomers: In geometrical isomers, atoms have different arrangements on either side of a double bond above or below the ring of a cycloalkane or cycloalkane. If the atoms are present on the same side of the double bond, then it is cis-isomer and if they are present on the opposite side of the double bond, then it is trans-isomer.
(a)
Answer to Problem 11.8E
The systematic name of the compound
Cis-
Explanation of Solution
The given compound is,
The compound is identified as alkene. The parent chain of the compound is pentane and a double bond is seen at the carbon second position. Hence, the systematic name of the compound is
Cis-
(b)
Interpretation:
The systematic name of the compound
Concept Introduction:
Refer to part (a).
(b)
Answer to Problem 11.8E
The systematic name of the compound
The geometrical isomers are not possible in
Explanation of Solution
The given compound is,
The compound is identified as alkene. The parent chain of the compound is butane. One methyl group is present in the carbon second position and a double bond is seen at the carbon second position. Hence, the systematic name of the compound is
No geometrical isomers are possible in
(c)
Interpretation:
The systematic name of the compound
Concept Introduction:
Refer to part (a).
(c)
Answer to Problem 11.8E
The systematic name of the compound
No geometrical isomers are possible in
Explanation of Solution
The given compound is,
The compound is identified as alkene. The parent chain of the compound is pentane. One methyl group is present in the carbon second position and a double bond is seen at the carbon second position. Hence, the systematic name of the compound is
No geometrical isomers are possible in
(d)
Interpretation:
The systematic name of the compound
Concept Introduction:
Refer to part (a).
(d)
Answer to Problem 11.8E
The systematic name of the compound
No geometrical isomers are possible in
Explanation of Solution
The given compound is,
The compound is identified as alkyne. The parent chain of the compound is heptane. One triple bond is present in carbon first position and one methyl substituent is present in carbon fourth position. Hence, the systematic name of the compound is
Geometrical isomers are not possible because triple bond has only one substituent each.
(e)
Interpretation:
The systematic name of the compound
Concept Introduction:
Refer to part (a).
(e)
Answer to Problem 11.8E
The systematic name of the compound
No geometrical isomers are possible in
Explanation of Solution
The given compound is,
The compound is identified as alkyne. The parent chain of the compound is heptane. One triple bond is present in carbon third position and one methyl substituent is present in carbon fifth position. Hence, the systematic name of the compound is
Geometrical isomers are not possible because triple bond has only one substituent each.
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Chapter 11 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
- Butanal (C4H&O) has eight H atoms. Suppose that any of these H atoms can be replaced by a Cl atom to yield a molecule with the formula C4H¬CIO. (a) Identify two H atoms where this substitution would yield constitutional isomers of C4H7CIO; (b) enantiomers of C4H;CIO; (c) conformers of C4H;CIO. H. H H H нн H Butanal O=Uarrow_forwardDraw the structures of the following compounds. (a) 1-isobutyl-4-isopropylcyclohexane; (b) tert-butylcyclopentane;(c) 3,3-diisopropyloctanearrow_forwardWrite structural formulas for compounds that meet the following descriptions:(a) An alkene, C6H12, that cannot have cis–trans isomersand whose longest chain is 5 carbons long(b) An alkene with a chemical formula of C10H12 that hascis–trans isomers and contains a benzene ring.arrow_forward
- sketch the various conformational isomers of 1,3-dimethylcyclohexane. Indicate the position (axial/equatorial) of each of the methyl groups in each structure.arrow_forwardWrite an equation to show the proton transfer between each alkene or cycloalkene and HCl. Where two carbocations are possible, show each. (a) CH,CH,CH=CHCH, (b) 2-Pentene Cyclohexenearrow_forwardDraw the structure(s) of all of the branched alkene isomers, C6H12, that contain 2 methyl branches.arrow_forward
- An alkane, P, has the molecular formula, C,H.. An alkene, Q, has the molecular formula, C H,. (a) Name P and Q ánd write their full structural formulae. (b) State two differences between P and Q in terms of their structures. x'arrow_forwardCyclopropane (C3H6, a three-membered ring) is more reactive than most other cycloalkanes.(a) Draw a Lewis structure for cyclopropane.(b) Compare the bond angles of the carbon atoms in cyclopropane with those in an acyclic (noncyclic) alkane.(c) Suggest why cyclopropane is so reactive.arrow_forwardA compound C3H6O has a hydroxyl group but no doublebonds. Write a structural formula consistent with thisinformation.arrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning