Concept explainers
(a)
Interpretation:
IUPAC name of the given cycloalkene has to be given.
Concept Introduction:
Naming of Cycloalkene using
Use the Cycloalkane name as the parent.
Cycloalkenes are named as alkyl-substituted cycloalkenes rather than as cycloalkyl-substituted
Identify and number the substituents.
The group which has alphabetical priority should be numbered first and proceed around the ring in a direction in which the double bond gets the lowest possible number.
(b)
Interpretation:
IUPAC name of the given cycloalkene has to be given.
Concept Introduction:
Naming of Cycloalkene using IUPAC nomenclature:
Use the Cycloalkane name as the parent.
Cycloalkenes are named as alkyl-substituted cycloalkenes rather than as cycloalkyl-substituted alkenes.
Identify and number the substituents.
The group which has alphabetical priority should be numbered first and proceed around the ring in a direction in which the double bond gets the lowest possible number.
(c)
Interpretation:
IUPAC name of the given cycloalkene has to be given.
Concept Introduction:
Naming of Cycloalkene using IUPAC nomenclature:
Use the Cycloalkane name as the parent.
Cycloalkenes are named as alkyl-substituted cycloalkenes rather than as cycloalkyl-substituted alkenes.
Identify and number the substituents.
The group which has alphabetical priority should be numbered first and proceed around the ring in a direction in which the double bond gets the lowest possible number.
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Chapter 5 Solutions
ORGANIC CHEMISTRY-OWL V2 ACCESS
- For each of the following compounds, identify all groups that would be considered substituents and then indicate the systematic name for each compound. (a) (b) (d) (e)arrow_forward(a) which if the structure of trans-1,2-dimethylcyclopentane? (b) which is the most stable conformation of 1-bromo-2-ethylcyclohexane? (c) which is the least stable conformation of 1-bromo-2-ethylcyclohexane? (d) which is the more stable configuration of 1,3-dimethylcyclopentane? *Et = ethylarrow_forwardName the following molecules according to the IUPAC nomenclature system. Indicate stereochemistry where appropriate. (a) CH,OCH,CH3 Br ČH3 (b) CIarrow_forward
- Consider the tricyclic structure A. (a) Label each substituent on the rings as axial or equatorial. (b) Draw a skeletal structure for A, using wedges and dashes to show whether the substituents are located above or below the rings.arrow_forwardGive the IUPAC names for each of the following compounds. a) b) c) Brarrow_forward(a) Are compounds B–D identical to or an isomer of A? (b) Give the IUPAC name for A.arrow_forward
- Provide IUPAC names for the compounds below.arrow_forwardThe skeletal line formula for a branched alkene is shown below. (i) What is the molecular formula of this compound? (ii) How many carbon atoms are in the longest chain, ignoring the double bond? (iii) What is the longest chain incorporating both carbons of the double bond? (iv) How many substituents are on this chain? (v) Give the IUPAC name for this compound. [6]arrow_forwardUse a Newman projection about the indicated bond to draw the most stable conformer for each compound. (a) 3-methylpentane about the C2¬C3 bondarrow_forward
- Draw the structures that correspond to their IUPAC or common name. (c) 4-mercapto-1-butanol (d) trans-1,3-diethoxycyclopentanearrow_forwardName each of these compounds according to the IUPAC system, Including stereochemistry. a) b) c) d) er CHz Cearrow_forward1. Name the following molecules according to the IUPAC nomenclature system. Indicate stereochemistry where appropriate. (a) CH2OCH,CH3 Br Cl CH3 oSH (b) Clarrow_forward
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning