Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 3.3, Problem 10P
Interpretation Introduction
a) Two tertiary carbons
Interpretation:
The structures of the
Concept introduction:
- Primary carbons are carbons attached to one carbon.
- Secondary carbons are attached to two other carbons.
- Tertiary carbons are attached to three other carbons.
- Finally, quaternary carbons are attached to four other carbons.
Interpretation Introduction
b) Isopropyl group
Interpretation:
The structures of the alkanes containing the following groups are to be drawn.
Concept introduction:
- Primary carbons are carbons attached to one carbon.
- Secondary carbons are attached to two other carbons.
- Tertiary carbons are attached to three other carbons.
- Finally, quaternary carbons are attached to four other carbons.
Interpretation Introduction
c) One quaternary and one secondary carbons
Interpretation:
The structures of the alkanes containing the following groups are to be drawn.
Concept introduction:
- Primary carbons are carbons attached to one carbon.
- Secondary carbons are attached to two other carbons.
- Tertiary carbons are attached to three other carbons.
- Finally, quaternary carbons are attached to four other carbons.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
Give the molecular formula of a hydrocarbon containingsix carbon atoms that is (a) a cyclic alkane, (b) a cyclicalkene, (c) a linear alkyne, (d) an aromatic hydrocarbon.
Provide ALL the rest of the constitutional isomers of hexane, and then NAME them
Are there alkene isomers with the molecular formula C2H3Cl?
Chapter 3 Solutions
Organic Chemistry
Ch. 3.1 - Prob. 1PCh. 3.1 - Prob. 2PCh. 3.1 - Identify the functional groups in the following...Ch. 3.2 - Draw structures of the five isomers of C6H14.Ch. 3.2 - Propose structures that meet the following...Ch. 3.2 - Prob. 6PCh. 3.3 - Draw the eight 5-carbon alkyl groups (pentyl...Ch. 3.3 - Identify the carbon atoms in the following...Ch. 3.3 - Prob. 9PCh. 3.3 - Prob. 10P
Ch. 3.4 - Give IUPAC names for the following compounds:Ch. 3.4 - Prob. 12PCh. 3.4 - Name the eight 5-carbon alkyl groups you drew in...Ch. 3.4 - Give the IUPAC name for the following hydrocarbon,...Ch. 3.7 - Make a graph of potential energy versus angle of...Ch. 3.7 - Sight along the C2-C1 bond of 2-methylpropane...Ch. 3.7 - Sight along the C2-C3 bond of 2,3-dimethylbutane,...Ch. 3.7 - Draw a Newman projection along the C2-C3 bond of...Ch. 3.SE - Prob. 19VCCh. 3.SE - Prob. 20VCCh. 3.SE - Draw a Newman projection along the C2-C3 bond of...Ch. 3.SE - Prob. 22APCh. 3.SE - Prob. 23APCh. 3.SE - Propose structures for the following: (a) A...Ch. 3.SE - Prob. 25APCh. 3.SE - Draw the structures of the following molecules:...Ch. 3.SE - Draw structures that meet the following...Ch. 3.SE - Prob. 28APCh. 3.SE - In each of the following sets, which structures...Ch. 3.SE - There are seven constitutional isomers with the...Ch. 3.SE - Prob. 31APCh. 3.SE - Draw compounds that contain the following: (a) A...Ch. 3.SE - Prob. 33APCh. 3.SE - Draw and name all monochloro derivatives of...Ch. 3.SE - Draw structures for the following: (a)...Ch. 3.SE - Prob. 36APCh. 3.SE - Draw a compound that: (a) Has nine primary...Ch. 3.SE - Give IUPAC names for the following compounds:Ch. 3.SE - Name the five isomers of C6H14.Ch. 3.SE - Explain why each of the following names is...Ch. 3.SE - Prob. 41APCh. 3.SE - Consider 2-methylbutane (isopentane). Sighting...Ch. 3.SE - What are the relative energies of the three...Ch. 3.SE - Construct a qualitative potential-energy diagram...Ch. 3.SE - Prob. 45APCh. 3.SE - Draw the most stable conformation of pentane,...Ch. 3.SE - Draw the most stable conformation of...Ch. 3.SE - Prob. 48APCh. 3.SE - Prob. 49APCh. 3.SE - Formaldehyde, H2C=O, is known to all biologists...Ch. 3.SE - Prob. 51APCh. 3.SE - Increased substitution around a bond leads to...Ch. 3.SE - Prob. 53APCh. 3.SE - In the next chapter we'll look at...Ch. 3.SE - We’ll see in the next chapter that there are two...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Draw all possible isomers of heptane, C7H16, and give their corresponding names.arrow_forwardDraw and name the five cycloalkane structures of formula C5H10. Can any of these structures give rise to geometric (cis-trans) isomerism? If so, show the cis and trans stereoisomersarrow_forwardDraw the structures and give the name of the 8 constitutional isomers withe the molecular formula C9H12 that contain a benzene ring.arrow_forward
- Give the molecular formula of a hydrocarbon containingfive carbon atoms that is (a) an alkane, (b) a cycloalkane,(c) an alkene, (d) an alkyne.arrow_forwardDetermine the DOU for the following molecules and suggest a structure for each. C5H7Br2ONarrow_forwardWhich of the following structural features could be found in a compound with formula C7H12?arrow_forward
- An unknown organic compound is found on elementalanalysis to contain 68.1% carbon, 13.7% hydrogen, and18.2% oxygen by mass. It is slightly soluble in water. Uponcareful oxidation it is converted into a compound thatbehaves chemically like a ketone and contains 69.7% carbon,11.7% hydrogen, and 18.6% oxygen by mass. Indicatetwo or more reasonable structures for the unknown.arrow_forwardFor each of the following compounds,determine whether each is optically active. For optically active compounds, identify the chiral carbon: ethane, 2-chloro-2-methylbutane, CH3CH(NH2)COOH, CH3CH2CHClCH3and CH3CH2CH2CH3. And for non-optical active compounds, just provide the structure of the compoundarrow_forwardWhat is an isomer having the formula C6H12 ?Without using 2-hexenearrow_forward
- One mole of an unknown hydrocarbon, compound C, in the presence of a platinum catalyst, adds 98.9 L of hydrogen, measured at 744 mm Hg and 22 degrees C , to form a saturated alkane which contains one ring. When one mole of compound C is reacted with ozone, followed by reduction with (CH3)2S , four moles of only one product was formed, whose condensed molecular formula is CHO -CHO. Give the structure of compound C. Explain your reasoningarrow_forwardC12H17O2N ----> CH3I gives ( in structural formula ) ?arrow_forwardThere are 11 structures (ignoring stereoisomerism) with the formula C4H8O that have no carbon branches. Draw the structures and identify the functional groups in each.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning