An the box, draw the resonance hybrid for cinnamaldebyde. Be sure your drawing indicates the location of every partial bond and every partial charge. On scratch paper you will need to draw out the different resonance forms in order to build the hybrid, but only draw the hybrid here. The o bond framework is provided. H. H. Cinnamaldehyde
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- I am having trouble on part c. It wants me to draw the resonance structure, but in mastering chem there’s no arrows available for some reason . Is there a way to draw it without the arrows and still be resonanceCurved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the resonance hybrid contributor. Include all lone pairs and charges as appropriate. Drawing Ⓒ2. Each resonance structure of a given molecule contributes to the resonance hybrid. The more stable the resonance structure, the more that resonance structure contributes to the resonance hybrid. For the following resonance structures, a. Circle the resonance structure that contributes most to the resonance hybrid. b. Explain your choice for a in complete sentences. c. Draw the resonance hybrid. d. Add curved arrows to indicate the flow of electrons in each structure except the D. H A Q Search B hyji C D
- 3. Provide ALL resonance contributors for the molecules I and II below. (Include the original structure provided below to start your answer.) For each molecule, draw the actual resonance hybrid structure indicating the atoms that carry a partial charge using the & symbol. You do NOT need to provide a numerical value of the partial charge. a. :0 :O: да b. C. taipII. Problem solving. 1. Choose from each pair the one that will exhibit the given property to the greater extent a. bond polarity N-H b. net number of lone pairs NH3 c. bond length CI-F d. formal charge on N e. net number of lone pairs f. bond strength g. bond polarity h. bond length electronegativity i. j. formal charge on O NH4+ NH₂™ C-O H-CI N-N O H₂O 2. Draw the Lewis structures of the following then evaluate the formal charge a. PBr3 b. CH3OH B-F CH4 F-F NH3 NH₁+ C-N H-F N = N CI H3O+ C. NO₂¹¹. Draw the indicated number of contributing resonance structures for the following compounds. Use curved arrows to show how to get from one resonance structure to the next. Lone pairs are not shown so you will have to put them in. Also, keep track of formal charges (7) (draw 3 additional structures) B. (draw 2 additional structures) C. (draw 2 additional structures)
- answer 3 and 5. PLS MAKE IT LIKE THIS WAY SO THAT I UNDERSTAND IT IONIC YES OR NO POLAR YES OR NO NON POLAR YES OR NO IMF EXIST IS..... NO EXPLANATION NEEDED.A. Choose the letter of the best answer. 1. What is a saturated hydrocarbon? A. Any compound consisting of carbon and hydrogen only. B. Any compound consisting of carbon and hydrogen and oxygen only. C. Any compound consisting of carbon and hydrogen only, in which some of the carbon atoms are joined to each other by double or triple bonds. D. Any compound consisting of carbon and hydrogen only, in which all the carbon atoms are joined to each other by single bonds. 2. What kind of hydrocarbon is C3H14? A. alkane C. alkyne B. alkene D. alcohol H. H H. 3. This molecule is an example of an... H. A. alkane C. alkyne B. alkene D. alcohol 4. Which is an example of an ether? А. CН3ОН B. CH3CH2CH2CI C. CH3CH2OCH2CH3 D. CH3CH2COOCH3 5. What is the simplest organic compound? A. methane C. ethanol B. acetone D. ethaneBenzene is the simplest member of a whole class of compounds called aromatic hydrocarbons. benzene a. How is each carbon atom hybridized? b. What is the geometry around each carbon atom? What is the overall geometry of the benzene ring? c. Draw a diagram showing the orbitals used to join the carbon atoms of the ring. d. Follow the indicated curved arrow notation to draw a second resonance structure. e. Benzene and other aromatic hydrocarbons are shown in Chapter 17 to be very stable. Offer an explanation.
- Meet benzylpenicillin, a common antibiotic for bacterial infections. Answer the following parts about this compound. a. Label all the functional groups present. b.For every heteroatom (i.e.atoms that are not CorH),predict the expected hybridization. c.Circle every carbon with a hydrogen capable of participating in hyperconjugation with a double bond. d.Draw one key resonance structure for each functional group capable of resonance, and one resonance hybrid with partial charges as applicable. e. Give the IUPAC name for this compound. Just kidding! It’s 3,3-dimethyl-7- oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid. Now, sit back and appreciate the limitations of naming—it’s only useful insofar as we understand each other.Draw the best LS (with lowest formal charges) for BeAt2 on a sheet of paper (NOT TO BE TURNED IN) and answer the following:(NOTE: Use the cardinal numbers 0, 1, 2, 3, and so on for any quantity required)a) give the number of lone electron pairs on Be atom. pairsb) give the number of lone electron pairs on each At atom. pairsc) what types of bonds are attached to Be? (choose correct letter from A – D): A. two double bonds C. two single bonds B. a single & double bond D. a double & triple bond d) Fill in the table below for BeAt2. For prediction of the actual bond angle, if the angle is ideal give the numerical value; if the angle is different from ideal use > (greater than) or < (less than) with the numerical value of the ideal bond angle (for e.g., < 1800). { NOTE: i) The correct spelling of the names matters. Be sure to check your spelling.ii) For the hybridization, place the superscript numbers on the same level as the letters. For…Click the "draw structure" button to launch the drawing utility. Using the curved arrow to guide your reasoning, draw the missing product of the following dissociation. Include formal charges and unshared electron pairs. Check your answer to ensure that charge is conserved. H H X. H H draw structure ...