Fundamentals of General, Organic, and Biological Chemistry (8th Edition)
8th Edition
ISBN: 9780134015187
Author: John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. Peterson
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 12.6, Problem 12.13P
(a)
Interpretation Introduction
Interpretation:
The condensed and line structure of
Concept introduction:
- Condensed structure: A shorthand way of drawing structures in which C-C and C-H bonds are understood rather than shown.
- Line structure is a simple and quick way to represent organic molecules without showing carbons and hydrogens present.
- Carbon can be classified into four types; they are primary (has one other carbon attached), secondary (has two other carbon attached), tertiary (has three other carbon attached) and quaternary (four other carbon attached.)
(b)
Interpretation Introduction
Interpretation:
The condensed and line structure of
Concept introduction:
- Condensed structure: A shorthand way of drawing structures in which C-C and C-H bonds are understood rather than shown.
- Line structure is a simple and quick way to represent organic molecules without showing carbons and hydrogens present.
- Carbon can be classified into four types; they are primary (has one other carbon attached), secondary (has two other carbon attached), tertiary (has three other carbon attached) and quaternary (four other carbon attached.)
(c)
Interpretation Introduction
Interpretation:
The condensed and line structure of
Concept introduction:
- Condensed structure: A shorthand way of drawing structures in which C-C and C-H bonds are understood rather than shown.
- Line structure is a simple and quick way to represent organic molecules without showing carbons and hydrogens present.
- Carbons can be classified into three types; they are primary (has one other carbon attached), secondary (has two other carbon attached), tertiary (has three other carbon attached) and quaternary (four other carbon attached.)
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Draw structures corresponding to the following names:(a) 3-Methylhexan-1-ol (b) 1-Methyl-3-propylcyclopentanol(c) 2,2-Dimethylhexan-3-ol (d) Heptan-3-ol(e) 2,3-Diethylcyclohexanol
Draw the structures of the following acids:(a) 2-Ethyl-3-hydroxyhexanoic acid (b) m-Nitrobenzoic acid
Which of the following define the stereochemistry of alanine (as per the structure shown)? Note: Functional groups arranged horizontally are facing towards the front, and the functional groups arranged vertically are facing towards the back.
a) d-
b) S-
c) R-
d) I-
Chapter 12 Solutions
Fundamentals of General, Organic, and Biological Chemistry (8th Edition)
Ch. 12.2 - Locate and identify the functional groups in (a)...Ch. 12.2 - Draw structures for molecules that fit the...Ch. 12.3 - Prob. 12.3PCh. 12.3 - There are two branched-chain isomers with the...Ch. 12.4 - Draw the following three isomers of C5H12 as...Ch. 12.4 - Prob. 12.6PCh. 12.4 - Prob. 12.7PCh. 12.4 - Draw both condensed and line structures for the...Ch. 12.5 - Which of the following structures represent the...Ch. 12.5 - Are the pairs of compounds shown below the same...
Ch. 12.6 - Identify each carbon in the molecule shown in...Ch. 12.6 - Prob. 12.12PCh. 12.6 - Prob. 12.13PCh. 12.6 - Draw and name alkanes that meet the following...Ch. 12.6 - Prob. 12.15KCPCh. 12.6 - Prob. 12.1CIAPCh. 12.6 - Prob. 12.2CIAPCh. 12.6 - Prob. 12.3CIAPCh. 12.8 - Prob. 12.1MRPCh. 12.8 - Prob. 12.2MRPCh. 12.8 - Prob. 12.16PCh. 12.8 - Write the structures of all singly chlorinated...Ch. 12.10 - Prob. 12.18PCh. 12.10 - Prob. 12.19PCh. 12.10 - What is wrong with the following names? It will be...Ch. 12.10 - Prob. 12.21KCPCh. 12.10 - Prob. 12.4CIAPCh. 12.10 - (a) What common produce items might you see...Ch. 12 - Convert the following models into line drawings...Ch. 12 - Prob. 12.23UKCCh. 12 - Prob. 12.24UKCCh. 12 - Give the IUPAC names for the following...Ch. 12 - Prob. 12.26UKCCh. 12 - What characteristics of carbon make possible the...Ch. 12 - Prob. 12.28APCh. 12 - Prob. 12.29APCh. 12 - Prob. 12.30APCh. 12 - For each of the following, give an example of a...Ch. 12 - Identify the highlighted functional groups in the...Ch. 12 - Identify the functional groups in the following...Ch. 12 - Propose structures for molecules that fit the...Ch. 12 - Prob. 12.35APCh. 12 - What requirement must be met for two compounds to...Ch. 12 - Prob. 12.37APCh. 12 - Prob. 12.38APCh. 12 - Prob. 12.39APCh. 12 - Prob. 12.40APCh. 12 - Give an example of a compound that meets the...Ch. 12 - (a)There are two isomers with the formula C4H10....Ch. 12 - Write condensed structures for the following...Ch. 12 - Prob. 12.44APCh. 12 - Prob. 12.45APCh. 12 - Which of the following pairs of structures are...Ch. 12 - Prob. 12.47APCh. 12 - Prob. 12.48APCh. 12 - Prob. 12.49APCh. 12 - What are the IUPAC names of the following alkanes?Ch. 12 - Prob. 12.51APCh. 12 - Write condensed structures for the following...Ch. 12 - Draw line structures for the following...Ch. 12 - Name the following cycloalkanes:Ch. 12 - Prob. 12.55APCh. 12 - Prob. 12.56APCh. 12 - Prob. 12.57APCh. 12 - Prob. 12.58APCh. 12 - Prob. 12.59APCh. 12 - Prob. 12.60APCh. 12 - Prob. 12.61APCh. 12 - Write the formulas of the four singly chlorinated...Ch. 12 - Write the formulas of the three doubly brominated...Ch. 12 - Identify the indicated functional groups in the...Ch. 12 - The line structure for pregabalin (Lyrica) is...Ch. 12 - Prob. 12.66CPCh. 12 - Prob. 12.67CPCh. 12 - Most lipsticks are about 70% castor oil and wax....Ch. 12 - Prob. 12.69CPCh. 12 - Prob. 12.70CPCh. 12 - Prob. 12.71CPCh. 12 - Which of the following structures represent the...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biochemistry and related others by exploring similar questions and additional content below.Similar questions
- Spermaceti, a fragrant substance isolated from sperm whales, was commonly used in cosmetics until it was banned in 1976 to protect the whales from extinction. Chemically, spermaceti is cetyl palmitate, the ester of palmiticacid with cetyl alcohol (the straight-chain 16-carbon alcohol). Draw the structure of spermaceti.arrow_forwardWrite chemical names for the following compounds: (a) Thymidine (b) Cytosine (c) Uracil (d) Xanthine (e) Guanine () 2,4-dioxy-6-carboxy pyrimidine (g) CAMP (h) dTTParrow_forwardDraw structures corresponding to the following names:(a) 2,4-Dimethylheptan-2-ol(b) 2,2-Diethylcyclohexanol(c) 5-Ethyl-5-methylheptan-1-ol(d) 4-Ethylhexan-2-ol(e) 3-Methoxycyclooctanol(f) 3,3-Dimethylheptane-1,6-diolarrow_forward
- Draw the structures of the following compounds. (Includes both new and old names.) 3-cyclopentylhexan-3-olarrow_forwardThe explosive trinitrotoluene (TNT) is made by carrying out three successive nitration reactions on toluene. If these nitrations only occur in the ortho and para positions relative to the methyl group, what is the structure of TNT?arrow_forward(A) What are Waxes? Draw the structure of wax, which is made up of palmitic acid (16:0) and a saturated 18-carbon alcohol. (В) Consider the structure of menthol. How many isoprene units are present in menthol? (C) What type of isoprene linkage (head-to-tail or tail-to-tail) is present in menthol? Identify the isoprene linkage in the following structure of menthol and indicate by a circle. Menthol =arrow_forward
- Are the following molecules chiral or achiral? If they are chiral, identify the chiral carbon atom(s).(a) Pentan-3-ol (b) 2-Bromobutane(c) 2-Methylcyclohexanolarrow_forwardFor A, B, C, D, E, F, identify the circled functional groups and linkages in the compound in the picture.arrow_forwardA) Describe the glycosidic bond (using standard convention) indicated by “Arrow a.” B) Draw the open chain Fischer projection formula of the monosaccharide labeled “B” C) Describe the glycosidic bond (as in question A) indicated by “Arrow b.”arrow_forward
- Draw the two possible Haworth structures (both alpha and beta anomers) for the following monosaccharides and give their corresponding systematic names. [Show the stepwise process]arrow_forwardShown below is the structure of guanine. -NH N NH₂ -N H Draw the potential tautomers of guanine. Explain the potential risk of guanine (enol form) during S phase. (i) (ii) N ΙΖarrow_forwardWhen Alfred Werner was developing the field of coordination chemistry, it was argued by some that the optical activity he observed in the chiral complexes he had prepared was due to the presence of carbon atoms in themolecule. To disprove this argument, Werner synthesized a chiral complex of cobalt that had no carbon atoms in it, and he was able to resolve it into its enantiomers. Design a cobalt(III) complex that would be chiral if it could be synthesized and that contains no carbon atoms.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- BiochemistryBiochemistryISBN:9781319114671Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.Publisher:W. H. FreemanLehninger Principles of BiochemistryBiochemistryISBN:9781464126116Author:David L. Nelson, Michael M. CoxPublisher:W. H. FreemanFundamentals of Biochemistry: Life at the Molecul...BiochemistryISBN:9781118918401Author:Donald Voet, Judith G. Voet, Charlotte W. PrattPublisher:WILEY
- BiochemistryBiochemistryISBN:9781305961135Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougalPublisher:Cengage LearningBiochemistryBiochemistryISBN:9781305577206Author:Reginald H. Garrett, Charles M. GrishamPublisher:Cengage LearningFundamentals of General, Organic, and Biological ...BiochemistryISBN:9780134015187Author:John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. PetersonPublisher:PEARSON
Biochemistry
Biochemistry
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:W. H. Freeman
Lehninger Principles of Biochemistry
Biochemistry
ISBN:9781464126116
Author:David L. Nelson, Michael M. Cox
Publisher:W. H. Freeman
Fundamentals of Biochemistry: Life at the Molecul...
Biochemistry
ISBN:9781118918401
Author:Donald Voet, Judith G. Voet, Charlotte W. Pratt
Publisher:WILEY
Biochemistry
Biochemistry
ISBN:9781305961135
Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougal
Publisher:Cengage Learning
Biochemistry
Biochemistry
ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Cengage Learning
Fundamentals of General, Organic, and Biological ...
Biochemistry
ISBN:9780134015187
Author:John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. Peterson
Publisher:PEARSON