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- 1. What is resonance contributor in which one or more atoms bears a formal change and the most stable resonance form? 2.what is the process of distributing electron pairs in a molecule? 3. Are organic molecules which are less sterically hindered more attractive than those which are more sterically hindered?4. The full structural formula of three organic compounds, P, Q and R, are shown below. H H HHH H HHHH H- C-C- H H C C-C = C- H H C C C C-H H H H H H. a. State one similarity between P, Q and R in terms of their molecular formula. b. Name the homologous series that compounds P, Q and R belong to. c. State one similarity between Q and R in terms of chemical bonding. d. Which of these compounds are isomers? Explain your answer.8. Draw a non-cyclic isomer of C3H6N2 in which the atom connectivity is N-C-C–C-N, and the middle C–C–C unit does NOT have a bond angle of 180°.
- What is the structure of this molecule using this HNMR? C7H16O242. Which of the following is not a functional isomer? A. CH,OH H НА a H Me B. C. D. Me H -ОН OH (A) O CH, CH, 0 CH3 OCH, (B) 43. Which of the following has a zero dipole moment? Choose the best answer. CI OH O CH, CH, (B) O H 1-1 C CI 44. Which of the following exhibits geometric isomerism? OH (C) (C) OH (D) 45. Which would be the most stable conformation of trans-1-ethyl-3-methylcylcohexane? (D) OH4. Assign R and S nomenclature to the chiral carbon atoms CI H. OCH3 а. с. b. HOH2C" `COOH CI
- 1. What type of reaction that all organic compounds undergo? 2. What is the total bond order of sulfur in CH3SCH3? 3. Explain the meaning in organic formulas of a pair of parentheses with no subscript behind it, such as in CH3CH2CH(CH3)C3H7H. H. Н H-C-C-0-Ċ-H | H H Н condensed structure: || CH3-CH2-O-CH3Which structure is correct? O SBr2 .S. Br Br: O N2 :NEN: OPH4 H. O CH3NH3 H. N H.
- 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 SOM2. Name the following molecules using IUPAC systematic naming, ignore stereochemistry. a. b. C. d. g. h. ex 8ء محكمه لار 3. Identify the hybridization (sp, sp2, sp³) of each carbon atom in the following molecules. } NH₂ 4. Identify the number of a bonds, bonds, lone pairs, and hydrogens in the following molecules. 8 1111 11111. How many carbon and hydrogen atoms are in the following molecule? Draw in all the lone pairs to complete the bond line structure. HS 2. Draw bond-line (skeletal) structures for all constitutional isomers of C4H10. 3. Draw the bond-line structure for the following condensed structures: (CH3)2CHCH2OC(CH3)3 CH;CH2CH2COCH2CH3 (CH3)2CHCOOH