Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 1.4, Problem 1.2P
Draw Lewis structures for the following compounds.
- a. ammonia, NH3
- b. water, H2O
- c. hydronium ion, H3O+
- d. propane. C3H8
- e. dimethylamme, CH3NHCH3
- f. diethyl ether, CH3CH2OCH2CH3
- g. 1-chloropropane, CH3CH2CH2C1
- h. propan-2-ol, CH3CH(OH)CH3
- i. borane, BH3
- j. boron trifluoride, BF3
Explain what is unusual about the bonding in the compounds in parts (i) and (j)
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Students have asked these similar questions
Part 1) If 3.36 moles of N2 and 3.90 moles of H2 are combined under,
which would be considered the limiting reactant?
Part 2) How many grams of NH will be formed during the reaction?
Part 3) In sufficient detail, describe the most valid Lewis structure of
NH3 (types of bonds, presence of unbonded electrons, existence of
any formal charges etc.), then specify its molecular geometry.
Based on the reaction to form ammonia (NH3
1) What do you predict the average bond length and average bond energy values for the F-F bond based on the chart below? WIll it be higher than, lower than, or the same as the other bonds shown in the chart. Justify your answer.
Bond
Average Bond Length (PM)
Average Bond Energy (KJ/MOLE)
CL-CL
199
243
Br-Br
228
193
I-I
267
151
2) Explain how a stable covalent bond is formed in terms of attractive and repulsive forces.
Note: Please briefly explain, Thank you.
Draw Lewis structures for the following compounds.(a) ammonia, NH3 (b) water, H2O(c) hydronium ion, H3O+ (d) propane, C3H8(e) dimethylamine, CH3NHCH3 (f) diethyl ether, CH3CH2OCH2CH3(g) 1-chloropropane, CH3CH2CH2Cl (h) propane-2-ol, CH3CH(OH)CH3(i) borane, BH3 (j) boron trifluoride, BF3Explain what is unusual about the bonding in the compounds in parts (i) and (j)
Chapter 1 Solutions
Organic Chemistry (9th Edition)
Ch. 1.2C - a. Nitrogen has relatively stable isotopes...Ch. 1.4 - Draw Lewis structures for the following compounds....Ch. 1.5 - Write Lewis structures for the following molecular...Ch. 1.5 - Circle any lone pairs (pairs of nonbonding...Ch. 1.6 - Use electronegativities to predict the direction...Ch. 1.8 - Prob. 1.6PCh. 1.9B - Draw the important resonance forms for the...Ch. 1.9B - Prob. 1.8PCh. 1.9B - Prob. 1.9PCh. 1.9B - Use resonance structures to identify the areas of...
Ch. 1.10A - Draw complete Lewis structures for the following...Ch. 1.10B - Give Lewis structures corresponding to the...Ch. 1.10B - Prob. 1.13PCh. 1.11 - Compute the empirical and molecular formulas for...Ch. 1.16 - a. Use your molecular models to make ethane, and...Ch. 1.17 - a. Predict the hybridization of the oxygen atom in...Ch. 1.17 - Predict the hybridization geometry and bond angles...Ch. 1.17 - Predict the hybridization, geometry, and bond...Ch. 1.17 - Prob. 1.19PCh. 1.17 - Allene, CH2=C=CH2, has the structure shown below...Ch. 1.17 - 1. Draw the important resonance forms for each...Ch. 1.18B - Prob. 1.22PCh. 1.18B - Two compounds with the formula CH3CH=NCH3 are...Ch. 1.19B - Prob. 1.24PCh. 1.19B - Give the relationship between the following pairs...Ch. 1 - a. Draw the resonance forms for SO2 (bonded OSO)....Ch. 1 - Name the element that corresponds to each...Ch. 1 - Prob. 1.28SPCh. 1 - For each compound, state whether its bonding is...Ch. 1 - a. Both PCl3 and PCl5 are stable compounds Draw...Ch. 1 - Draw a Lewis structure for each species a. N2H4 b....Ch. 1 - Prob. 1.32SPCh. 1 - Prob. 1.33SPCh. 1 - Draw Lewis structures for a. two compounds of...Ch. 1 - Prob. 1.35SPCh. 1 - Some of the following molecular formulas...Ch. 1 - Prob. 1.37SPCh. 1 - Give the molecular formula of each compound shown...Ch. 1 - 1. From what you remember of electronegativities,...Ch. 1 - For each of the following structures, 1. Draw a...Ch. 1 - Prob. 1.41SPCh. 1 - Prob. 1.42SPCh. 1 - Prob. 1.43SPCh. 1 - Prob. 1.44SPCh. 1 - For each pair of ions, determine which on is more...Ch. 1 - Use resonance structures to identify the areas of...Ch. 1 - Prob. 1.47SPCh. 1 - In 1934, Edward A. Doisy of Washington University...Ch. 1 - If the carbon atom in CH2Cl2 were fat. there would...Ch. 1 - Cyclopropane (C3H6, a three-membered ring) is more...Ch. 1 - Prob. 1.51SPCh. 1 - Prob. 1.52SPCh. 1 - In most amines, the nitrogen atom is sp3...Ch. 1 - Predict the hybridization and geometry of the...Ch. 1 - Draw orbital pictures of the pi bonding in the...Ch. 1 - Prob. 1.56SPCh. 1 - Prob. 1.57SPCh. 1 - Which of the following compounds show cis-trans...Ch. 1 - Give the relationships between the following pairs...Ch. 1 - Dimethyl sulfoxide (DMSO) has been used as an...
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