1.) Draw two constitutional isomers that share the molecular formulas а.) С,Н.Р b.) C,H¿N c.) C,H,0 2.) Carbon-hydrogen bonds exhibit a range of different chemical reactivity that depends on molecular structure. Classify the C-H bonds at the carbons labeled a-c in the structure below. Possible classifications are: primary, secondary, & tertiary or none if there are no hydrogens at the labeled carbon. a b а.) b.) b a с.) 3.) Draw a structural formula for 3-ethylnonane.
1.) Draw two constitutional isomers that share the molecular formulas а.) С,Н.Р b.) C,H¿N c.) C,H,0 2.) Carbon-hydrogen bonds exhibit a range of different chemical reactivity that depends on molecular structure. Classify the C-H bonds at the carbons labeled a-c in the structure below. Possible classifications are: primary, secondary, & tertiary or none if there are no hydrogens at the labeled carbon. a b а.) b.) b a с.) 3.) Draw a structural formula for 3-ethylnonane.
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
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![1.) Draw two constitutional isomers that share the molecular formulas
а.) С,Н.Р
b.) C,H¿N
c.) C,H,0
2.) Carbon-hydrogen bonds exhibit a range of different chemical reactivity that depends on molecular structure.
Classify the C-H bonds at the carbons labeled a-c in the structure below. Possible classifications are: primary,
secondary, & tertiary or none if there are no hydrogens at the labeled carbon.
a
b
а.)
b.)
b
a
с.)
3.) Draw a structural formula for 3-ethylnonane.
а.) CН4](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe5309a50-92ea-42e3-946e-c637f882638a%2F749fddc7-bf83-406f-98e9-696a4e0b7a9c%2Fm9ynckt_processed.png&w=3840&q=75)
Transcribed Image Text:1.) Draw two constitutional isomers that share the molecular formulas
а.) С,Н.Р
b.) C,H¿N
c.) C,H,0
2.) Carbon-hydrogen bonds exhibit a range of different chemical reactivity that depends on molecular structure.
Classify the C-H bonds at the carbons labeled a-c in the structure below. Possible classifications are: primary,
secondary, & tertiary or none if there are no hydrogens at the labeled carbon.
a
b
а.)
b.)
b
a
с.)
3.) Draw a structural formula for 3-ethylnonane.
а.) CН4
![4.) Write the IUPAC name for the compound below. Be sure to use correct punctuation.
CH3
CH3-CH-CH2-CH2-CH3
a.)
The IUPAC name is
ÇH2-CH2-CH3
CH3-CH2-CH2-CH2-ĊH-CH2-CH2-CH3
b.)
The IUPAC name is
c.) Keep the information page open for guidance and for use with feedback. Accepted names for branched
alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. Do not use italics.
CH2CH2CH3
CH3CH2ĊCH2CH3
ČH3
The IUPAC name is
5.) Draw the structure of a.) 3-ethyl-5-methyloctane and b.) 5-tert-butyl-3-ethyl-6-isopropylnonane. You do not
have to explicitly draw H atoms.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe5309a50-92ea-42e3-946e-c637f882638a%2F749fddc7-bf83-406f-98e9-696a4e0b7a9c%2Fx2jt1a1_processed.png&w=3840&q=75)
Transcribed Image Text:4.) Write the IUPAC name for the compound below. Be sure to use correct punctuation.
CH3
CH3-CH-CH2-CH2-CH3
a.)
The IUPAC name is
ÇH2-CH2-CH3
CH3-CH2-CH2-CH2-ĊH-CH2-CH2-CH3
b.)
The IUPAC name is
c.) Keep the information page open for guidance and for use with feedback. Accepted names for branched
alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. Do not use italics.
CH2CH2CH3
CH3CH2ĊCH2CH3
ČH3
The IUPAC name is
5.) Draw the structure of a.) 3-ethyl-5-methyloctane and b.) 5-tert-butyl-3-ethyl-6-isopropylnonane. You do not
have to explicitly draw H atoms.
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