ORGANIC CHEMISTRY
6th Edition
ISBN: 9781266633973
Author: SMITH
Publisher: MCG
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Chapter 1, Problem 82P
The N atom in
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Chapter 1 Solutions
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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- The structure of amphetamine, a stimulant, is shown below. (Replacing one H atom on the NH2, or amino, group with CH3 gives methamphetamine a particularly dangerous drug commonly known as speed.) (a) What are the hybrid orbitals used by the C atoms of the C6 ring. by the C atoms of the side chain, and by the N atom? (b) Give approximate values for the bond angles A, B, and C. (c) How many bonds and bonds are in the molerule? (d) Is the molecule polar or nonpolar? (e) Amphetamine reacts readily with a proton (H+) in aqueous solution. Where does this proton attach to the molecule? Explain how the electrostatic potential map predicts this site of protonation.arrow_forwardThe sulfamate ion, H2NSO3, can be thought of as having been formed from the amide ion, NH2, and sulphur trioxide, SO3. (a) What are the electron-pair and molecular geometries or the amide ion and or SO3? What are the hybridizations of the N and S atoms, respectively? (b) Sketch a structure for the sulfamate ion, and estimate the bond angles. (c) What changes in hybridization do you expect for N and S in the course of the reaction NH2 + SO3 H2NSO3? (d) Is SO3 the donor of an electron pair or the acceptor of an electron pair in the reaction with amide ion? Does the electrostatic potential map shown below confirm your prediction?arrow_forwardAspirin, or acetylsalicylic acid, has the formula C9H8O4 and the skeleton structure (a) Complete the Lewis structure and give the number of bonds and bonds in aspirin. (b) What is the hybridization about the CO2H carbon atom (colored blue)? (c) What is the hybridization about the carbon atom in the benzene-like ring that is bonded to an oxygen atom (colored red)? Also, what is the hybridization of the oxygen atom bonded to this carbon atom?arrow_forward
- Draw the Lewis structure for 1, 1-dimethylhydrazine [(CH3)2NNH2, a compound used as a rocket fuel]. What: is the hybridization for the two nitrogen atoms in this molecule? What orbitals overlap to form the bond between the nitrogen atoms?arrow_forwardAcetic acid can be made by the oxidation of acetaldehyde(CH3CHO). Molecules of acetaldehyde have a-CH3 group, an oxygen atom, and a hydrogen atom attached to a carbon atom. Draw the Lewis diagram for this molecule, give the hybridization of each carbon atom, and describethe p orbitals and the number of electrons that occupy each one. Draw the three-dimensional structure of the molecule, showing all angles.arrow_forwardC2H6 and HI State the type of hybridization (sp, sp", etc) for the central atom in each molecule. Show how the various single, double and/or triple bonds form in each of the molecules. Make use of orbital diagrams, labels, and/or written sentences in your explanation.arrow_forward
- Draw a Lewis diagram(s) for the ozone molecule (O3). Determine the steric number and hybridization of the central oxygen atom, and identify the molecular geometry. Describe the nature of the p bonds and give the bondorder of the O-O bonds in ozone.arrow_forwardIn ozone, O3, the two oxygen atoms on the ends of the molecule are equivalent to one another. (a)What is the best choice of hybridization scheme for the atoms of ozone? (b) For one of the resonance forms of ozone, which of the orbitals are used to make bonds and which are used to hold nonbonding pairs of electrons? (c) Which of the orbitals can be used to delocalize the π electrons? (d) How many electrons are delocalized in the π system of ozone?arrow_forwardwe considered the electronic structure of [CH2NH2]+. Predict its hybridization, geometry, and bond angles.arrow_forward
- (a) What is the hybridization of chlorine in Clo4 ? (Type your answer using the format sp3 for sp3.) (b) What is the hybridization of bromine in BrF5? (c) What is the hybridization of bromine in BrO2 ?arrow_forwardDraw the Lewis structure of the molecule. What do you predict for the bond order of the C¬S bonds?arrow_forwardDraw the molecular orbital energy diagrams for the valence electrons in the following diatomic molecules. Calculate the bond order and indicate if each of them is diamagnetic or paramagnetic. (а) В> (b) С. (c) CO (d) NO (е) Оzarrow_forward
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