Study Guide/solutions Manual For Organic Chemistry
6th Edition
ISBN: 9781260475678
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Chapter 1, Problem 72P
Two useful organic compounds that contain
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A chemist wants to observe the following reaction:
2H2 + O2 → 2H2O
The chemist is standing inside a room with oxygen in the air and has a balloon filled with hydrogen. The chemist holds a small flame up to the hydrogen balloon. When the balloon pops, the hydrogen explodes in a ball of fire.
Based on what you know about breaking and forming bonds, explain which part of the reaction is higher in energy (i.e., does it take more energy to break the bonds of the reactants, or is more energy given off when the product bonds are formed?). Defend your answer in three to five sentences.
Carbon-carbon bonds form the “backbone” of nearly every organic and biological molecule. The average bond energy of the C¬C bond is 347 kJ/mol. Calculate the frequency and wavelength of the least energetic photon that can break an average C¬C bond. In what region of the electromagnetic spectrum is this radiation?
The compound oxygen difluoride is quite reactive, giving oxygen and HF when treated with water:
OF2(g) + H2O(g) → O2(g) + 2HF(g)
ΔE°rxn = –318 kJ
Using bond energies, calculate the bond dissociation energy of the O–F bond in OF2.
Average Bond Energies (kJ/mol)
Picture
O–F bond dissociation energy = _____kJ/mol
Chapter 1 Solutions
Study Guide/solutions Manual For Organic Chemistry
Ch. 1.1 - While the most common isotope of nitrogen has a...Ch. 1.2 - Label each bond in the following compounds as...Ch. 1.3 - Draw a valid Lewis structure for each species. a....Ch. 1.3 - Prob. 9PCh. 1.4 - Draw Lewis structures for each molecular formula....Ch. 1.6 - Classify each pair of compounds as isomers or...Ch. 1.6 - Prob. 12PCh. 1.6 - Prob. 13PCh. 1.6 - Prob. 14PCh. 1.6 - Prob. 16P
Ch. 1.6 - Prob. 17PCh. 1.7 - Prob. 18PCh. 1.7 - Prob. 19PCh. 1.7 - Using the principles of VSEPR theory, you can...Ch. 1.8 - Convert each condensed formula to a Lewis...Ch. 1.8 - Prob. 22PCh. 1.8 - Prob. 23PCh. 1.8 - Convert each skeletal structure to a complete...Ch. 1 - Citric acid is responsible for the tartness of...Ch. 1 - Zingerone gives ginger its pungent taste. a.What...Ch. 1 - Assign formal charges to each and atom in the...Ch. 1 - Prob. 44PCh. 1 - Prob. 46PCh. 1 - Draw all possible isomers for each molecular...Ch. 1 - 1.45 Draw Lewis structures for the nine isomers...Ch. 1 - Prob. 52PCh. 1 - Prob. 53PCh. 1 - Prob. 54PCh. 1 - Consider compounds A-D, which contain both a...Ch. 1 - Draw in all the carbon and hydrogen atoms in each...Ch. 1 - 1.61 Convert each molecule into a skeletal...Ch. 1 - Prob. 65PCh. 1 - Predict the hybridization and geometry around each...Ch. 1 - Prob. 68PCh. 1 - Ketene, , is an unusual organic molecule that has...Ch. 1 - Rank the following bonds in order of increasing...Ch. 1 - Two useful organic compounds that contain Cl atoms...Ch. 1 - Use the symbols + and to indicate the polarity of...Ch. 1 - Prob. 74PCh. 1 - Anacin is an over-the-counter pain reliever that...Ch. 1 - 1.77 Stalevo is the trade name for a medication...Ch. 1 - 1.78 and are two highly reactive carbon...Ch. 1 - 1.79 The N atom in (acetamide) is hybridized,...Ch. 1 - Prob. 83PCh. 1 - Prob. 84PCh. 1 - Prob. 85PCh. 1 - Prob. 86PCh. 1 - Prob. 87PCh. 1 - Prob. 88P
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- Two compounds have the molecular formula N3H3. One of the compounds, triazene, contains an NN bond; the other compound, triaziridene, does not. (a) Write the correct Lewis structures for each compound. (b) Approximate the bond angle between the three nitrogen atoms in each compound.arrow_forwardAnswer the questions in the table below about the shape of the trichlorostannanide How many electron groups are around the central tin atom? Note: one "electron group" means one lone pair, one single bond, one double bond, or one triple bond. What phrase best describes the arrangement of these electron groups around the central tin atom? (You may need to use the scrollbar to see all the choices.) 0 (choose one) X S SnC13) anion.arrow_forwardAlthough carbon has four bonds in stable molecules, sometimes reactive carbon intermediates that contain carbon atoms without four bonds are formed for very short time periods. Examples of these unstable intermediates include the methyl carbocation (CH 3) + and the methyl carbanion (CH 3) −. Draw Lewis structures for both unstable ions and predict the shape around carbon.arrow_forward
- In addition to CO, CO2, and C3O2, there is another molecular oxide of carbon, pentacarbon dioxide, C5O2, a yellow solid. (a) What is the approximate C-to-C-to-O bond angle in pentacarbon dioxide? (b) What is the approximate C-to-C-to-C bond angle in this compound?arrow_forwardBond Enthalpy When atoms of the hypothetical element X are placed together, they rapidly undergo reaction to form the X2 molecule: X(g)+X(g)X2(g) a Would you predict that this reaction is exothermic or endothermic? Explain. b Is the bond enthalpy of X2 a positive or a negative quantity? Why? c Suppose H for the reaction is 500 kJ/mol. Estimate the bond enthalpy of the X2 molecule. d Another hypothetical molecular compound, Y2(g), has a bond enthalpy of 750 kJ/mol, and the molecular compound XY(g) has a bond enthalpy of 1500 kJ/mol. Using bond enthalpy information, calculate H for the following reaction. X2(g)+Y2(g)2XY(g) e Given the following information, as well as the information previously presented, predict whether or not the hypothetical ionic compound AX is likely to form. In this compound, A forms the A+ cation, and X forms the X anion. Be sure to justify your answer. Reaction: A(g)+12X2(g)AX(s)The first ionization energy of A(g) is 400 kJ/mol. The electron affinity of X(g) is 525 kJ/mol. The lattice energy of AX(s) is 100 kJ/mol. f If you predicted that no ionic compound would form from the reaction in Part e, what minimum amount of AX(s) lattice energy might lead to compound formation?arrow_forwardThe hyponitrite ion, ONNO, exists in solid compounds as the trans isomer. Using valence bond theory, explain why cistrans isomers might be expected for this ion. Draw structural formulas of the cistrans isomers.arrow_forward
- (a) Draw a Lewis structure for the ozone molecule, O3. (The order of atom attachment is OOO, and they do not form a ring.) Chemists use ozone to cleave carbon-carbon double bonds (Section 6.5C). (b) Draw four contributing resonance structures; include formal charges. (c) How does the resonance model account for the fact that the length of each OO bond in ozone (128 pm) is shorter than the OO single bond in hydrogen peroxide (HOOH, 147 pm) but longer than the OO double bond in the oxygen molecule (123 pm)?arrow_forwardBest Lewis Formula and Molecular Geometry A student writes the Lewis electron-dot formula for the carbonate anion, CO32, as a Does this Lewis formula obey the octet rule? Explain. What are the formal charges on the atoms? Try describing the bonding for this formula in valence bond terms. Do you have any difficulty doing this? b Does this Lewis formula give a reasonable description of the electron structure, or is there a better one? If there is a better Lewis formula, write it down and explain why it is better. c The same student writes the following resonance description for CO2: Is there something wrong with this description? (What would you predict as the geometries of these formulas?) d Is one or the other formula a better description? Could a value for the dipole moment help you decide? e Can you write a Lewis formula that gives an even better description of CO2? Explain your answer.arrow_forwardWhat is the approximate ClCCl bond angle in phosgene, COCl2? (Carbon is the central atom in this compound.) (a) 90 (b) 109.5 (c) 120 (d) 180arrow_forward
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