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- Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position in benzonitrile. CEN benzonitrile • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the chloro with the para position in chlorobenzene. 0 chlorobenzene • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one. . 99-85 On [F ChemDoodleⓇThe following is generic depiction of a reaction using the curve arrow formalism. -D Which of these statements is not correct for this reaction? Electrons move from C to B. Electrons move from B to A. O In the products, a bond forms between C and B. O In the products, A would have a positive charge.
- [Review Topics] Draw a structural formula for 2,2-dichlorocycloheptanol. • Show stereochemistry only if given in the name. • If a group is achiral, do not use wedged or hashed bonds on it. • In cases where there is more than one answer, just draw one. P. opy aste [F ChemDoodleIn the following acid - base reactions, a) Draw Lewis structures of the reactants and the products. b) Determine which species are acting as electrophiles (acids) and which are acting as nucleophiles (bases). c) Use the curved - arrow formalism to show the movement of electron pairs in these reactions and the imaginary movement in the resonance hybrids of the products. d) Indicate which reactions are best termed Brønsted-Lowry acid - base reactions i. CH3CHO + HCI-- > CH3CH2O + + Cl- ii. CH3CHO + OH- - - > CH3CO-(OH) H3.) HAI(CH,CH(CH3)2l2 (DIBAL-H) 1.) NBS 2.) NaCN 4.) H, H20 Thermodynamic Product Br a) 1.) b.) 1.) c.) 1.) Br Br 2) 2) 2) CN CN CN 3.) 3.) 3.) 4) 4) H. NH2
- ! ( give step by step explanation)o. Opioids are compounds derived from opium, which comes from the opium poppy. Although in reality, all poppies produce opoids, the drug “morphine" , codeine as well as other opioid pain killers are typically derived from opium. A quick way to find or identify these compounds is to look for a six-membered ring containing a nitrogen. Often, if you see a six-membered ring with a nitrogen, you have some sort of an opoid or a modified synthetic pain killer. With that said, morphine and codeine are typically not injected or given orally in pure form. Instead, their salts are used, such as morphine sulfate or codeine phosphate. Why are the salts used or administered instead of the pure substances (or non-salt forms)? (I am not interested in drug names, but to have you answer the why of this question.) BIU E E E E 3回fe 27 В. acen W 1 F T F2 F3 F4 F5 F6 F7 F8 F9 F10 F11 F12 () NumLk Prt Sc Pause Brte Bb Welcome, Kawtha... O Maps GE News Home [Review Topics)] [References] Draw structural formulas for the major organic product(s) of the reaction shown below. CH2CH3 stered FeBr3 Br2 You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. • Remember to include all of the formal charges on the atoms of any nitro groups. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. opy aste Previous Next Email Instructor Save and Cengage Learning | Cengage Technical Support
- 1 i. What is Resonance Theory? Sate five conclusions that can be drawn from the theory. ii. State the two main experiments that were used to establish the extra stability of the benzene molecule. iii. What are the factors that confer Aromaticity to an organic molecule? iv. State the effects of substituents on a benzene derivative towards further aromatic substitution. V. Based on the above suggest the various types of substituents that can be attached to Benzene.Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the amino with the ortho position in aniline. NH₂ aniline • You do not have to consider stereochemistry. Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. ● / // Sn [F ?4. Resonance. For each of the following structural formulas, provide the indicated number of resonance structures. Use curved arrows to show the electron movement between each structure, use double headed arrow to separate the structures, and enclose all of them in a single set of brackets []. a) N204 (O₂N-NO2) (4 structures)