Principles of General, Organic, Biological Chemistry
2nd Edition
ISBN: 9780073511191
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 10, Problem 10.41AP
Complete each structure by filling in all H’s and lone pairs.
- a. C—C=C—C
- b. C=C—C—O
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Fill in all H's and lone pairs in each compound.
b. c--c
а. С—С—с—С
С. С —С—С
d. C-Ĉ-N-C
е.
Convert each condensed formula to a Lewis structure.
a. CH3(CH2)4CH(CH3)2
b. (CH3)3CCH(OH)CH2CH3
c. (CH3)2CHCHO
d. (HOCH2)2CH(CH2)3C(CH3)2CH2CH3
Which of the following compounds is a valid Lewis structure of a hydrocarbon?
H
H-C-Ö-H
H
HH
H-C-N-H
H
I
II
H
H-C-C-H
H
III
HH
H-C-C-H
I
НН
IV
I, II, and IV are valid structures of hydrocarbons.
Only III is a valid structure of hydrocarbons.
All of these compounds are valid structures of hydrocarbons.
Only IV is a valid structure of hydrocarbons.
III and IV are valid structures of hydrocarbons.
Chapter 10 Solutions
Principles of General, Organic, Biological Chemistry
Ch. 10.1 - Prob. 10.1PCh. 10.2 - Fill in all Hs and lone pairs in each compound. a....Ch. 10.3 - Convert each compound to a condensed formula.Ch. 10.3 - Convert each condensed formula to a complete...Ch. 10.3 - Convert each skeletal structure to a complete...Ch. 10.3 - How many Hs are bonded to each indicated carbon...Ch. 10.4 - Identify the functional groups in each compound....Ch. 10.4 - For each compound: [1] Identify the functional...Ch. 10.4 - Prob. 10.9PCh. 10.4 - Prob. 10.10P
Ch. 10.4 - Convert the ball-and-stick model of the local...Ch. 10.5 - How many hydrogen atoms are present in each...Ch. 10.5 - Prob. 10.13PCh. 10.5 - Prob. 10.14PCh. 10.5 - Prob. 10.15PCh. 10.5 - Prob. 10.16PCh. 10.6 - Give the IUPAC name for each compound.Ch. 10.6 - Prob. 10.18PCh. 10.6 - Prob. 10.19PCh. 10.6 - Prob. 10.20PCh. 10.7 - Prob. 10.21PCh. 10.7 - Prob. 10.22PCh. 10.9 - Answer the following questions about pentane...Ch. 10.9 - Prob. 10.24PCh. 10.9 - Prob. 10.25PCh. 10.10 - Prob. 10.26PCh. 10 - Prob. 10.27UKCCh. 10 - Prob. 10.28UKCCh. 10 - Prob. 10.29UKCCh. 10 - Prob. 10.30UKCCh. 10 - Prob. 10.31UKCCh. 10 - The largest known cycloalkane with a single ring...Ch. 10 - Draw three constitutional isomers having molecular...Ch. 10 - Draw four constitutional isomers having molecular...Ch. 10 - Answer the following questions about the alkane...Ch. 10 - Answer the questions in Problem 10.35 for the...Ch. 10 - Prob. 10.37UKCCh. 10 - Procaine (trade name Novocain) is a local...Ch. 10 - Prob. 10.39APCh. 10 - Prob. 10.40APCh. 10 - Complete each structure by filling in all Hs and...Ch. 10 - Prob. 10.42APCh. 10 - Prob. 10.43APCh. 10 - Prob. 10.44APCh. 10 - Prob. 10.45APCh. 10 - Prob. 10.46APCh. 10 - Convert each compound to a condensed structure.Ch. 10 - Prob. 10.48APCh. 10 - Prob. 10.49APCh. 10 - Prob. 10.50APCh. 10 - Prob. 10.51APCh. 10 - Prob. 10.52APCh. 10 - Albuterol (trade names: Proventil and Ventolin) is...Ch. 10 - Prob. 10.54APCh. 10 - Prob. 10.55APCh. 10 - Prob. 10.56APCh. 10 - Prob. 10.57APCh. 10 - Prob. 10.58APCh. 10 - Prob. 10.59APCh. 10 - Prob. 10.60APCh. 10 - Prob. 10.61APCh. 10 - Prob. 10.62APCh. 10 - Prob. 10.63APCh. 10 - Prob. 10.64APCh. 10 - Prob. 10.65APCh. 10 - Prob. 10.66APCh. 10 - Prob. 10.67APCh. 10 - Prob. 10.68APCh. 10 - Prob. 10.69APCh. 10 - Prob. 10.70APCh. 10 - Give the IUPAC name for each compound.Ch. 10 - Prob. 10.72APCh. 10 - Prob. 10.73APCh. 10 - Prob. 10.74APCh. 10 - Prob. 10.75APCh. 10 - Prob. 10.76APCh. 10 - Give the structure corresponding to each IUPAC...Ch. 10 - Prob. 10.78APCh. 10 - Prob. 10.79APCh. 10 - Each of the following IUPAC names is incorrect....Ch. 10 - Prob. 10.81APCh. 10 - Prob. 10.82APCh. 10 - Prob. 10.83APCh. 10 - Prob. 10.84APCh. 10 - Prob. 10.85APCh. 10 - Prob. 10.86APCh. 10 - Write a balanced equation for the incomplete...Ch. 10 - Prob. 10.88APCh. 10 - Prob. 10.89APCh. 10 - Prob. 10.90APCh. 10 - Prob. 10.91APCh. 10 - Prob. 10.92APCh. 10 - Answer the following questions for the cycloalkane...Ch. 10 - Prob. 10.94APCh. 10 - Prob. 10.95CPCh. 10 - Prob. 10.96CP
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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
- Assign formal charges to each carbon atom in the given species. All lone pairs have been drawn in. H H Н— С, — Сь H H Ca (select) v Съ (select) varrow_forwardDraw the best Lewis structure of C₂0. Include lone pair electrons and any formal charges. Click and drag to start drawing a structure. C C X Ś C+arrow_forwardV. Give what is asked. 1. When 2 carbon atoms form a double bond, how many pairs of e- will be shared between them? 2. An alkane has 5 carbon atoms. How many hydrogen atoms will it have? 3. An alkene has 3 carbon atoms. How many hydrogen atoms will it have? 4. An alkyne has 4 carbon atoms. How many hydrogen atoms will it have? 5. Show the Lewis structure for the stable molecule CH3.arrow_forward
- How are the molecules or ions in each pair related? Classify them as resonance structures, isomers, or neither. CH3 a. CH,-Ö-CH,CH, and C. and b. and CH3-C=C-CH3 d. CH;CH,CH3 CH,CH,ČH2 and ннarrow_forward10. Write the structures obtained when electrons move as indicated by the curved arrows in the following structure. Does each atom in the resulting structure have a complete valence shell of electrons? Locate any formal charges in the new structure. Don't worry about arrows converting back to the original structure, just draw the new structure and include the appropriate formal charges, if needed. н Н- EN: Н Н. -CH3arrow_forwardWhich structure is correct? O SBr2 .S. Br Br: O N2 :NEN: OPH4 H. O CH3NH3 H. N H.arrow_forward
- B. Cycloalkanes 1) Construct a model of the cyclic alkane: cyclopentane (C5H₁0). Because the five carbon atoms are locked in a ring, rotation about the single bonds is restricted; the plane of the ring a fixed geometry within the molecule. Toggle between full Lewis structures and skeletal structures by clicking the C-H tool. Model 1: Use the solid wedge tool to attach a methyl group to each of two different carbon atoms in the cyclopentane. Note the five carbons of the ring are in the plane of the paper, and the solid wedge indicates both methyls project forward, in front of the plane of the paper. Model 2: Use the solid wedge tool to attach first methyl group to one of two different carbon atoms in the cyclopentane, and use the dashed wedge tool to attach the second. Note the solid wedge indicates that one methyl projects forward, in front of the plane of the paper. The dashed wedge indicates the other methyl extends back, behind the plane of the paper. Click the broom to tidy up the…arrow_forwardAlthough we usually don't show lone pairs on skeletal structures, sometimes it's necessary, for example, to show how a reaction will occur. Draw in any lone pairs in the structure below. Note: you may need to redraw parts of the structure to show atoms and bonds within a group before you can add any missing lone pairs ОН OH H,N H,N°arrow_forwardLine-bond structures appear to imply that there are two different isomers of 1,2-dibromobenzene, one with the bromine-bearing carbon atoms joined by a double bond and one with the bromine-bearing carbons joined by a single bond. In fact, though, there is only one 1,2-dibromobenzene. Explain. H H. C. Br H. .C. Br || || .C and 1,2-Dibromobenzene Br Brarrow_forward
- Ф -OH Identify the structure below that represent the same compound shown above O A. B. OC. OH OH .OH CI .CI CIarrow_forward5. Redraw the following structures below in Lewis form, filling in all of the implied carbon atoms and hydrogen atoms. 6. The following are the reagent, intermediate, and product in a reaction you will learn later in Organic Chemistry. a. Identify any formal charges that are missing from the structures. b. Draw in all lone pairs. c. Redraw the structures with all hydrogen atoms. to t OH ₂arrow_forwardAre these the same molecule? H H-C- same molecule isomers different molecules -N—H H Harrow_forward
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