
(a)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction:
In order to give the IUPAC name to the alcohol following steps are followed:
1. The parent (longest)
2. The ending of the parent chain from alkane (-e) is changed to -ol and the number is used to locate the -OH group of alcohol.
3. Name should be written in alphabetical order and numbering should be done in such a way that hydroxy group gets lowest number.
4. Configuration should be specified is there exist any cis-trans isomerism.
For number of carbons atoms in chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
(b)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction:
In order to give the IUPAC name to the alcohol following steps are followed:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -ol and the number is used to locate the -OH group of alcohol.
3. Name should be written in alphabetical order and numbering should be done in such a way that hydroxy group gets lowest number.
4. Configuration should be specified is there exist any cis-trans isomerism.
For number of carbons atoms in chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
(c)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction:
In order to give the IUPAC name to the alcohol following steps are followed:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -ol and the number is used to locate the -OH group of alcohol.
3. Name should be written in alphabetical order and numbering should be done in such a way that hydroxy group gets lowest number.
4. Configuration should be specified is there exist any cis-trans isomerism.
For number of carbons atoms in chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec

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Chapter 17 Solutions
Basic Chemistry
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- Identifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardAssign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forward
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