Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 16.2, Problem 16.1P
Interpretation Introduction
Interpretation: The Lewis structure for Kekule representations of benzene by representing all the valence electrons is to be stated.
Concept introduction: The diagrams that are used for representing bonding electrons and lone pairs that is present in a molecule. Valence electrons are the number of electrons that are present in the outermost shell of an atom.
To determine: The Lewis structure for Kekule representations of benzene by representing all the valence electrons.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
Write Lewis structures for the Kekulé representations of benzene. Show all the valenceelectrons.
Diazomethane (CH2N2) is an important reagent for the methylation of some organic molecules. Complete Parts 1 and 2 below about this unique reagent.
Draw the Lewis structure of diazomethane (CH2N2) that contains a formal charge on carbon and nitrogen. Be sure to include all lone pairs of electrons and formal charges.
Draw Lewis Structures for the following compounds. (Be sure to minimize formal charges and draw resonance structures where appropriate.): XeF2O, ClO4-, HNO2, CH3CH(NH2)COOH (amino acid alanine). Identify the molecules with the following labels (1 is more than one label): Oxyacid, has a resonance structure, expanded octet, has a carbon backbone For the molecule with resonance structures—what is the bond order for the atoms that share e-?
Chapter 16 Solutions
Organic Chemistry (9th Edition)
Ch. 16.2 - Prob. 16.1PCh. 16.2 - Prob. 16.2PCh. 16.2 - a. Draw the resonance forms of benzene,...Ch. 16.2 - Show the product of the Diels-Alder dimerization...Ch. 16.4 - Prob. 16.5PCh. 16.6 - Make a model of cyclooctatetraene in the tub...Ch. 16.6 - Prob. 16.7PCh. 16.6 - Prob. 16.8PCh. 16.7 - Prob. 16.9PCh. 16.8A - a. Draw the molecular orbitals for the...
Ch. 16.8A - Repeat Problem16-10 for the cyclopentadienyl ions....Ch. 16.8C - Explain why each compound or ion should be...Ch. 16.8C - The following hydrocarbon has an unusually large...Ch. 16.8C - Prob. 16.14PCh. 16.8C - Prob. 16.15PCh. 16.9B - Prob. 16.16PCh. 16.9C - Show which of the nitrogen atoms in purine are...Ch. 16.9C - The proton NMR spectrum of 2-pyridone gives the...Ch. 16.9D - Prob. 16.19PCh. 16.9D - Prob. 16.20PCh. 16.10 - Prob. 16.21PCh. 16.12 - Ciprofloxacin is a member of the fluoroquinolone...Ch. 16.13 - Draw and name all the chlorinated benzenes having...Ch. 16.13 - Name the following compounds:Ch. 16.15 - The UV spectrum of 1-phenylprop-2-en-1-ol shows an...Ch. 16 - Prob. 16.26SPCh. 16 - Name the following compounds:Ch. 16 - Draw and name all the methyl, dimethyl, and...Ch. 16 - Four pairs of compounds are shown. In each pair,...Ch. 16 - One of the following hydrocarbons is much more...Ch. 16 - In Kekuls time cyclohexane was unknown, and there...Ch. 16 - Prob. 16.32SPCh. 16 - Azulene is a deep-blue hydrocarbon with resonance...Ch. 16 - Prob. 16.34SPCh. 16 - Prob. 16.35SPCh. 16 - Prob. 16.36SPCh. 16 - Prob. 16.37SPCh. 16 - Prob. 16.38SPCh. 16 - Prob. 16.39SPCh. 16 - Biphenyl has the following structure. a. Is...Ch. 16 - Anions of hydrocarbons are rare, and dianions of...Ch. 16 - How would you convert the following compounds to...Ch. 16 - Prob. 16.43SPCh. 16 - Prob. 16.44SPCh. 16 - A student found an old bottle labeled thymol on...Ch. 16 - Prob. 16.46SPCh. 16 - Prob. 16.47SPCh. 16 - Prob. 16.48SPCh. 16 - The proton NMR chemical shifts of the hydrogens in...Ch. 16 - Prob. 16.50SPCh. 16 - NMR has been used to probe many molecular...
Knowledge Booster
Learn more about
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
- Two major resonance structures are possible for the anion shown. One resonance form is given, but it is incomplete. Complete the given structure by adding nonbonding electrons and formal charges. Draw the remaining structure, including nonbonding electrons and formal charges. Omit curved arrows. Structure A: complete the structure by adding nonbonding electrons and formal charges. H H H I Structure B: draw the remaining resonance structure, including nonbonding electrons and formal charges. H- : z: H Harrow_forwardIt is asking for second resonance structure. I think I did the second resonance structure wrong for each one. This is for organic chemistry.arrow_forwardIn the following Lewis structure of [SiF6]²;, every atom, bond and lone pair is positioned. To complete the structure, drag the formal charge tags to the appropriate atom(s). Each marker may be used more than once, or not at all. If an atom has a formal charge of zero, do not drag a tag to it. When you drag the marker in, place the little crosshairs in the upper left corner of the marker directly over the atom(s) in question (not above them). :F: :F: 2+ 2- :L: :L:arrow_forward
- Draw the Lewis dot structure of the conjugate base of cyclopentane by assuming all the atoms in the molecule obey the octet rule. Show all lone pairs and formal charges. Do no draw resonance structures.arrow_forward1. For each of the following compounds and ions, draw the complete Lewis structure. All formal charges should be on the atoms that possess that formal charge. CH4 H3CBr CH3CH₂OH H₂S H₂SO4 (sulfuric acid) H³0+ CH3* 2. Convert the following condensed formulas into bond-line structures, making sure to draw in zig-zag formation. CH3CH₂CH₂CH₂CH₂CH₂CH₂CH3 FCH₂CH₂I H₂C=CHCH₂OH (CH3)2CHCOOHarrow_forwardADVANCED MATERIAL Interpreting condensed chemical structures Use this condensed chemical structure to complete the table below. CH,= CH- CH= CH, The condensed chemical structure of 1,3-butadiene Some facts about the 1,3-butadiene molecule: number of carbon-carbon single (C - C) bonds: number of carbon-hydrogen single (C - H) bonds: number of carbon-carbon double (C = C) bonds: te Roserved.arrow_forward
- Draw the best resonance structure for cyanic acid HOCN . Be sure to include all lone pair electrons and nonzero formal charges. The skeletal arrangement is given as follows.arrow_forwardDraw the Lewis structure for formaldehyde, CH2O. Include all hydrogens and lone pairs explicitly.arrow_forwardDetermine the best Lewis structure for acetonitrile. Include the formal charge carbon and nitrogen atom. on eacharrow_forward
- In the following Lewis structure of [(CH3)2OH]*, every atom, bond and lone pair is positioned. To complete the structure, drag the formal charge tags to the appropriate atom(s). Each marker may be used more than once, or not at all. If an atom has a formal charge of zero, do not drag a tag to it. When you drag the marker in, place the little crosshairs in the upper left corner of the marker directly over the atom(s) in question (not above them). H. H-C Н-С-О-С-Н C-H H HH 2- II 2-arrow_forwardThree major contributing resonance structures are possible for the following cation. One is given below. Draw the remaining structures (in any order), including nonbonding electrons and formal charges. Omit curved arrows. н н CH3З Which contributes most to the hybrid? The structure with the positive charge on sulfur. All contribute equally. O The structures with the positive charge on carbon.arrow_forwardWrite a Lewis structure for each of the following molecules/ions. Be sure to show all non-zero formal charges. Start by counting the valence electrons.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
