Cycloheptatrienone is an unusually stable ketone. Draw an aromatic resonance structure that explains the stability. Include all lone pairs in your structure.
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- ew topic [References Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. H3C SCH3 • Include all valence lone pairs in your answer. • For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less- substituted carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the → symbol from the drop-down menu. C P opy aste 11:58 M 18 52% 4/11/2021Based on the image answer the following questions: H-C- FF FC a) What were these compounds used for in the late 1950s and 1960s? b) What is a pro of using these compounds compared to what was being used in the past? c) In the late 1980s and 1990s what has changed the metamorphosis of this compound?Please draw the structure CLEARLY so that I can understand it. Thanks
- With reference to structure A, label structure B as an identical compound, a constitutional isomer, a resonance structure, or none of the above. Select the single best answer. CI 519 O Constitutional isomer O Resonance structure O Identical compound O None of the above1. Determine whether the molecule below is: Phenol CI CI CI CI Bisphenol Biguanide Heavy metal Phenolic H CI ОН но CI Aldehyde (c) Hexachlorophene Gaseous Quaternary ammonium compound (quat) H-C-Please answer all of it. If not, please skip. Draw the structure of a branched hydrocarbon that also contains at least one atom with trigonal planar geometry. Draw the structure of an aromatic hydrocarbon containing two halogens. Draw the structure of a molecule containing an aliphatic primary amine and a carboxyl group. Draw the structure of an acyclic molecule containing a primary and a secondary alcohol group. Draw the structure of an achiral tertiary alcohol
- comparing to this two ketone, which ketone has the most stable π system? Explain on the basis of the carbonyl group.Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations are not needed. Keep it short, brief, and direct because I only need the answers. How are the following two molecules related to each other?Explain why phenols are more acidic than alcohols. Elaborate.
- Examine the IR below and classify the compound. Alcohol Aldehyde Carboxylic acid KetoneComplete the following statements so that they are true. Ry value. Ry value. R; value. Ry value. a. A more polar compound has a b. A less polar compound has a c. A more polar solvent causes a d. A less polar solvent causes a e. To increase the Ry of a spot, you should add more of which solvent, hexanes or ethyl acetate?Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Give the name of the following compound: