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 3.11, Problem 3.30P
Show the direction of the dipole in each bond. Label the atoms with δ+ and δ–.
- a. H—F
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Draw a resonance structure that places a pi bond in a different
position. Include all lone pairs in your structure.
H
HIN:
:O:
:O:
H
Atoms, Bonds
and Rings
H₂N
C
1
Arrange the highlighted bonds in the table below in decreasing order of polarity. That is, pick 1 for the most polar bond, pick 2 for the next most polar bond, and
so on.
bond
polarity
H-Ö-H
(Choose one)
H.
H-C-H
(Choose one)
H.
H-F:
(Choose one)
HIC
For each pair, indicate the more polar bond by circlingthe negative end of its dipole.a. C—S, C—Ob. C—F, C—Nc. P—H, P—Cl
Chapter 3 Solutions
Principles of General, Organic, Biological Chemistry
Ch. 3.1 - Predict whether the bonds in the following species...Ch. 3.2 - Write the ion symbol for an atom with the given...Ch. 3.2 - Prob. 3.4PCh. 3.2 - Prob. 3.5PCh. 3.2 - How many electrons and protons are contained in...Ch. 3.2 - Prob. 3.7PCh. 3.3 - Write the formula for the ionic compound formed...Ch. 3.3 - Prob. 3.9PCh. 3.4 - Prob. 3.10PCh. 3.4 - Give the symbol for each ion. a. stannous b....
Ch. 3.4 - Name each ionic compound. a. NaF b. MgO c. SrBr2...Ch. 3.4 - Name each ionic compound. a. CrCl3 b. PbS c. SnF4...Ch. 3.4 - Prob. 3.14PCh. 3.5 - List four physical properties of ionic compounds.Ch. 3.6 - Write the formula for the compound formed when K+...Ch. 3.6 - Prob. 3.17PCh. 3.6 - Name each compound. a. Na2CO3 b. Ca(OH)2 c....Ch. 3.6 - Prob. 3.19PCh. 3.7 - Use electron-dot symbols to show how a hydrogen...Ch. 3.7 - Prob. 3.21PCh. 3.8 - Draw a Lewis structure for each covalent molecule....Ch. 3.8 - Prob. 3.23PCh. 3.8 - Prob. 3.24PCh. 3.9 - Prob. 3.25PCh. 3.9 - Prob. 3.26PCh. 3.10 - Prob. 3.27PCh. 3.11 - Prob. 3.28PCh. 3.11 - Prob. 3.29PCh. 3.11 - Show the direction of the dipole in each bond....Ch. 3.12 - Prob. 3.31PCh. 3.12 - Prob. 3.32PCh. 3 - Which formulas represent ionic compounds and which...Ch. 3 - Which pairs of elements are likely to form ionic...Ch. 3 - Prob. 3.35UKCCh. 3 - Prob. 3.36UKCCh. 3 - Prob. 3.37UKCCh. 3 - Prob. 3.38UKCCh. 3 - Prob. 3.39UKCCh. 3 - Prob. 3.40UKCCh. 3 - Prob. 3.41UKCCh. 3 - Prob. 3.42UKCCh. 3 - Prob. 3.43UKCCh. 3 - Prob. 3.44UKCCh. 3 - Prob. 3.45UKCCh. 3 - Prob. 3.46UKCCh. 3 - (a) Translate each ball-and-stick model to a Lewis...Ch. 3 - Prob. 3.48UKCCh. 3 - Prob. 3.49APCh. 3 - How many protons and electrons are present in each...Ch. 3 - Prob. 3.51APCh. 3 - Prob. 3.52APCh. 3 - Prob. 3.53APCh. 3 - Give the ion symbol for each ion. a. barium ion b....Ch. 3 - Prob. 3.65APCh. 3 - Write the formula for the ionic compound formed...Ch. 3 - Prob. 3.67APCh. 3 - Prob. 3.68APCh. 3 - Name each ionic compound. a. Na2O b. BaS c. PbS2...Ch. 3 - Name each ionic compound. a. KF b. ZnCl2 c. Cu2S...Ch. 3 - Prob. 3.71APCh. 3 - Write formulas to illustrate the difference...Ch. 3 - Prob. 3.73APCh. 3 - Name each ionic compound. a. (NH4)2SO4 b. NaH2PO4...Ch. 3 - Prob. 3.75APCh. 3 - Prob. 3.76APCh. 3 - Prob. 3.77APCh. 3 - Label each statement as true or false. Correct any...Ch. 3 - Prob. 3.79APCh. 3 - Prob. 3.80APCh. 3 - Prob. 3.81APCh. 3 - Prob. 3.82APCh. 3 - Convert the 3-D model of oxalic acid into a Lewis...Ch. 3 - Convert the 3-D model of the general anesthetic...Ch. 3 - Prob. 3.85APCh. 3 - Prob. 3.86APCh. 3 - Prob. 3.87APCh. 3 - Prob. 3.88APCh. 3 - Prob. 3.89APCh. 3 - Prob. 3.90APCh. 3 - Prob. 3.91APCh. 3 - Prob. 3.92APCh. 3 - Prob. 3.93APCh. 3 - Prob. 3.94APCh. 3 - Rank the atoms in each group in order of...Ch. 3 - Prob. 3.96APCh. 3 - Prob. 3.97APCh. 3 - Prob. 3.98APCh. 3 - Prob. 3.99APCh. 3 - Which bond in each pair is more polarthat is, has...Ch. 3 - Prob. 3.101APCh. 3 - Prob. 3.102APCh. 3 - Isobutyl cyanoacrylate is used in medical glues to...Ch. 3 - Prob. 3.104APCh. 3 - Prob. 3.105CPCh. 3 - Prob. 3.106CP
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- Drag the symbol to indicate the correct relationship between the molecules. 4. Bond X-N-X bond angle CH3 H;C `CH3 5. C-O bond polarity 6. Strength of the sp³C-H bond NH H3C° `Cl H3C `Cl Varrow_forwardArrange the highlighted bonds in the table below in decreasing order of polarity. That is, pick 1 for the most polar bond, pick 2 for the next most polar bond, and so on. bond polarity H (Choose one) H H. H Н—с—н |(Choose one) H H-F: |(Choose one)arrow_forwardDraw a resonance structure that places a pi bond in a different position. Include all lone pairs in your structure. H HIN: :O: :O: Drawing J H 1 Oarrow_forward
- 1. Which is longer-a C-H bond or a C-O bond? 2. Which is shorter-an N-H bond or a C-H bond? 3. Arrange the following bonds from least polar to most polar: Н-О, H-F, H-N, H-CIarrow_forward4. Draw all resonance forms for the cation shown below. Include a resonance hybrid. +arrow_forward2. Which is shorter-an N-H bond or a C-H bond? 3. Arrange the following bonds from least polar to most polar: H-O, H-F, H-N, H-CIarrow_forward
- Draw a second resonance structure for each species in parts (a) and (b). Draw two additional resonance structures for the ion in part (c). ci: a. CH3 C H H I C H CH3 b. H H H c. CH3 :O: :O: II C. || C. I H CH3arrow_forwardDraw a resonance structure that places a pi bond in a different position. Include all lone pairs in your structure. I H. N | H :O: :0: Harrow_forwardFor each compound, determine the direction of bond polarity. Leave the box blank for a nonpolar bond. Br—Br H—Cl F—CH3arrow_forward
- b. There is one additional resonance structure. NH₂ c. There is a total of five resonance structures (including the original structure). : OHarrow_forwardArrange the highlighted bonds in the table below in decreasing order of polarity. That is, pick 1 for the most polar bond, pick 2 for the next most polar bond, and so on. bond polarity H-F: (Choose one) ▼ H-Ö-H (Choose one) (Choose one) H H.arrow_forwardents V Soul (TV series) O REPRESENTATIONS OF ORGANIC MOLECULES Drawing a skeletal structure from a Lewis structure Convert the Lewis structure below into a skeletal structure. Н—С— Н H. H- H- Н—С—Н H. HH H. H- Н—С—С—С—С—С—С—С- Н C=C H- H. H. H. Н—С— Н H. ct+ Click and drag to start drawing a structure. HIC CIH HICarrow_forward
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