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- 2. Identify and state any formal charges in the following structures. CH3 - CECH (I) 3. Draw any dipoles in the following structure. Draw your answers in question. 2. above. AH! 4-0 ㅍ CH3 on the structures shownBDE - Bund dissociaton Greigy. (1.CHsBr BOE 219Kcalmon & CH3CH2 Br BOE 187 kealonor- Cは。-CH-Br BDI 164 kealmor 4. Cuz- - Br 149 Kealmoj BDE blhich of has bond u easier to break! 2. ohy??Which of the following would you expect to be aromatic H. II III IV V I and II .a O Vb O IV II .d O е е W
- Which structure is the most stable NH₂ A. Br O NH₂ E. D. B. NH₂ NH₂ Y by x Br Rr Br C. Br NH₂5. Do the following structures represent resonance structures? If yes, identify them by stating the more stable and less stable. ? H ? c=0 b) H FCH2 H. H ? ? H-CE d) HConsider this reaction when answering the following question(s): H CH3 ہ سے ان H3C- b. C. :0: :0: H H CH3 acid catalyst H3C- :0: + a. The structures below show the step-wise bond making and bond breaking in this reaction. Draw curved arrows to show the electron flow that has occurred in each step. H H :0: :0: H- OH - - H Η Η H H Calculate Keq for the reaction in part a. Calculate AG for the reaction in part a. H + 76% ح H2 -ة: H 76% + H
- 3. Draw all possible significant resonance structures for the following: :ö : H. `NH2What are the configurations of the double bond and at the carbons marked C2 and C3 respectively? OH H3C Select one: O a. (E), (S), (S) O b. (E), (S), (R) O C. CH3 d. O e. O f. (E), (R), (S) (E), (R), (R) (Z), (S), (S) (Z), (R), (S) g. (Z), (S), (R) Oh. (Z), (R), (R) H3C 3 CH3 CH3 CH315. Draw all the important resonance structures for the following ion, and show all the lone pair of electrons and formal charges. Show the electron flow by using arOws. NH NH 16. Draw skeletal structures of compounds accordinghto he rules provided and write their common names 100 16b. drawskeletal 16c. draw skeletal 16d drawskeletal arawskeletal an ether that contains abenzer ing (No limit on the total rumber of carbons) a secondary alkyl chloride with 4 carbons total a primary alcohol with 4 carbons total a tertiary amine with 6 carbons total common name common name common name common name
- 1. Using the letter designations, consider the set of compounds below as you answer the following questions. H slo nobenin sdi in alluest disponojam od) wer B E 0= N a. Which of these compounds is/are aromatic? -NH -N d. What is the hybridization of the N atoms in compound I? Yoitiosqeed oitoso eidt ni olidgtosle leutos art ei tedW J e. What is the hybridization of the N atom in compound E? N= HN G Sboboon od bicow ansest ter b. Considering only compounds F, G, H and J and assuming all are planar, which is/are wel antiaromatic? c. Considering only compounds A, B, C, D and E, which is/are nonplanar? On SOMempt.php?attempt3D1101388&cmid%3D371560&page%3D2 Indicate the relationship between the following pair of compounds as same, structural isomers, geometrical isomers, resonance or different В. H,CO H3CO C. HN A BI 0 耳 !!!Draw all reasonable resonance structures for each species. a. O3 c. Ng e. g. :O: :O: b. NO, (a central N atom) d. CH3-C-CH-C-CH, 1. CH2=CH-CH-CH=CH2