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Concept explainers
(a)
Interpretation:
All resonance contributors for sulfuric acid
Concept introduction:
If a species having two or more valid Lewis structures, then its resonance structure exists. Resonance structures are imaginary; true species is represented by the resonance hybrid. The resonance structures are differed by the placement of their valence electrons, and not their atoms. Resonance structures with a greater number of atoms having an octet complete, more covalent bonds, and fewer atoms having a non-zero formal charge are considered to be stable. While drawing resonance structures curved arrows are used. The movement of a pair of electrons is indicated by a curved arrow. A curved arrow originates from a lone pair of electrons or from a covalent double or triple bond to indicate the specific pair of electrons that are being moved. The arrow points to an atom if the electrons being moved become a lone pair. Otherwise, the arrow points to the center of an existing bond to represent the formation of a new double/triple bond. A resonance structure can be drawn if a lone pair of electrons on an atom is adjacent with multiple bonds or an incomplete octet on an atom is adjacent to multiple bonds or there is a ring of alternating single and multiple bonds.
(b)
Interpretation:
Resonance hybrid for
Concept introduction:
A resonance hybrid structure is a weighted average structure of all the resonance contributors. A partial bond is represented in a resonance hybrid by a dashed line connecting the two atoms. In the resonance hybrid, the partial bonds are shown, which represent the atoms over which the electrons are delocalized. The resonance hybrid structure looks most like the lowest energy resonance structure and it is the most stable structure. The more stable resonance structures have a) a greater number of atoms having octet complete, b) more number of covalent bonds, and c) fewer atoms having a non-zero formal charge.
(c)
Interpretation:
The resonance structures of
Concept introduction:
A resonance hybrid structure is a weighted average structure of all the resonance contributors. A partial bond is represented in a resonance hybrid by a dashed line connecting the two atoms. In the resonance hybrid, the partial bonds are shown, which represent the atoms over which the electrons are delocalized. The resonance hybrid structure looks most like the lowest energy resonance structure and it is the most stable structure. The more stable resonance structures have a) a greater number of atoms having octet complete, b) more number of covalent bonds, and c) fewer atoms having a non-zero formal charge.
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Chapter 1 Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
- Transmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)arrow_forwardNonearrow_forwardDraw the Lewis structure of C2H4Oarrow_forward
- a) 5. Circle all acidic (and anticoplanar to the Leaving group) protons in the following molecules, Solve these elimination reactions, and identify the major and minor products where appropriate: 20 points + NaOCH3 Br (2 productarrow_forwardNonearrow_forwardDr. Mendel asked his BIOL 260 class what their height was and what their parent's heights were. He plotted that data in the graph below to determine if height was a heritable trait. A. Is height a heritable trait? If yes, what is the heritability value? (2 pts) B. If the phenotypic variation is 30, what is the variation due to additive alleles? (2 pts) Offspring Height (Inches) 75 67.5 60 52.5 y = 0.9264x + 4.8519 55 60 65 MidParent Height (Inches) 70 75 12pt v V Paragraph B IUA > AT2 v Varrow_forward
- Experiment: Each team will be provided with 5g of a mixture of acetanilide and salicylic acid. You will divide it into three 1.5 g portions in separate 125 mL Erlenmeyer flasks savıng some for melting point analysis. Dissolve the mixture in each flask in ~60mL of DI water by heating to boiling on a hotplate. Take the flasks off the hotplate once you have a clear solution and let them stand on the bench top for 5 mins and then allow them to cool as described below. Sample A-Let the first sample cool slowly to room temperature by letting it stand on your lab bench, with occasional stirring to promote crystallization. Sample B-Cool the second sample 1n a tap-water bath to 10-15 °C Sample C-Cool the third sample in an ice-bath to 0-2 °C Results: weight after recrystalization and melting point temp. A=0.624g,102-115° B=0.765g, 80-105° C=1.135g, 77-108 What is the percent yield of A,B, and C.arrow_forwardRel. Intensity Q 1. Which one of the following is true of the compound whose mass spectrum is shown here? Explain how you decided. 100 a) It contains chlorine. b) It contains bromine. c) It contains neither chlorine nor bromine. 80- 60- 40- 20- 0.0 0.0 TT 40 80 120 160 m/z 2. Using the Table of IR Absorptions how could you distinguish between these two compounds in the IR? What absorbance would one compound have that the other compound does not? HO CIarrow_forwardIllustrate reaction mechanisms of alkenes with water in the presence of H2SO4, detailing each step of the process. Please show steps of processing. Please do both, I will thumb up for sure #1 #3arrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
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