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3. Draw the other major resonance structure of the following compounds. (10 pts) o pphs pphs...
Problem 10. Draw the structure of the major product formed in each of the following reactions....
Problem 10. Draw the structure of the major product formed in each of the following reactions. Consider the resulting stereochemistry of the products formed (6p) KBr ng MeOH NaF DMSO H2(g), Pd (cat.) c) Solvent OH 1) NaH (strong base) THF (solvent) d) 2) CI Nal e) CI Acetone
3) Consider the following structure: a) (6 pts) Draw two additional resonance structures for the following...
3) Consider the following structure: a) (6 pts) Draw two additional resonance structures for the following compound. Show curved arrows to convert between the resonance structures. (You need to redraw the molecule below) b) (4 pts) Circle the major contributor above. Explain your choice 4) (5 pts) For the following compound draw in the lone pairs, indicate if each lone pair is localized or delocalized and identify what type of orbital each lone pair is in
14. Draw Lewis structures for the following compounds. If they exhibit resonance, draw one other resonance...
14. Draw Lewis structures for the following compounds. If they exhibit resonance, draw one other resonance structure for a total of two structures a. XeO,F2 b. NO, c. C,H, d. SO, e. SCI. f. KrF,
14. Draw Lewis structures for the following compounds. If they exhibit resonance, draw one other resonance...
14. Draw Lewis structures for the following compounds. If they exhibit resonance, draw one other resonance structure for a total of two structures. b. NO a. ХеО,F, d. SO с. С.Н, f. KrF e. SCI, 15. Draw three resonance structures of NO, in which the atoms are arranged in the order NNO. Indicate the formal charges in each.
(i). Draw the structure of the products for the following reactions: (3.5 x 2 = 7...
(i). Draw the structure of the products for the following reactions: (3.5 x 2 = 7 pts) NaHCO3 OOH Тон NaHCO3 (ii). Fill out the table below: (1.5 pt per box x 4 = 6 pts) Compounds Ionic/Polar/Non polar? Water Solubility? 0 OH Lotoon (iii). Name all the intermolecular forces of attraction present in the molecule below. (3 pts) (iv). Circle the most acidic protons in the following compounds: (2 x 2 = 4 pts)
1. (6 pts.) Rank the following compounds in order of increasing acidity. Each series should be co...
Please solve and explain
1. (6 pts.) Rank the following compounds in order of increasing acidity. Each series should be considered separately. Use resonance and/or inductive effects to explain acidity. For full credit you will need to draw any resonance forms or indicate dipole if it is relevant. Also for each compound draw its conjugate base. Series 1: OH он OH O Series 2: CN 2. (4 pts.) Fill the reactions with the products and circle the favorite side: OH+...
Draw the structure of following compounds 3. Draw the structure of following compounds. 4-Bromo 3- chlorobenzoic...
Draw the structure of following compounds
3. Draw the structure of following compounds. 4-Bromo 3- chlorobenzoic acid 4-Chlorobutyl-3-chloro hexanoate Isobutyl acetate MacBook Air esc F1 F2 20 F $ 4 2 3 % 5 & 7 6 & Pentandjoic acid Cyclo propane dicarboxylic aad MacBook Air F2 F3 FS 97 # $
1. Draw all the significant resonance forms for the following structures, and indicate which are major...
1. Draw all the significant resonance forms for the following structures, and indicate which are major and which are minor, or if you have two equally important forms, say so. The number of new forms you need to draw is shown in parentheses below the arrow. (a) N co 4. In each of the following reactions, indicate which structure is the nucleophile and which is the electrophile. Also draw the products (use the electron pair arrows to guide you). (a)...
1. Draw all resonance structures for the following compound. Circle the major contributor (to the resonance...
1. Draw all resonance structures for the following compound.
Circle the major contributor (to the resonance hybrid) and give a
brief explanation for your choice. (4 pts) 2. Determine the
configuration (show priorities and work) for any chiral centers in
the molecule below. (2 pts)
2. Determine the configuration (show priorities and work) for
any chiral centers in the molecule below. (2 pts)
1. Draw all resonance structures for the following compound. Circle the major contributor (to the resonance hybrid)...
4. Resonance: (10 pts) Sketch the additional resonance forms of the given structure. Include charges, resonance...
4. Resonance: (10 pts) Sketch the additional resonance forms of the given structure. Include charges, resonance arrows, and electron movement arrows. Circle the major resonance structure. If all structures are equivalent write 'same'. H. ΘΗ 4
Problem 10. Draw the structure of the major product formed in each of the following reactions. Consider the resulting stereochemistry of the products formed (6p) KBr ng MeOH NaF DMSO H2(g), Pd (cat.) c) Solvent OH 1) NaH (strong base) THF (solvent) d) 2) CI Nal e) CI Acetone
3) Consider the following structure: a) (6 pts) Draw two additional resonance structures for the following compound. Show curved arrows to convert between the resonance structures. (You need to redraw the molecule below) b) (4 pts) Circle the major contributor above. Explain your choice 4) (5 pts) For the following compound draw in the lone pairs, indicate if each lone pair is localized or delocalized and identify what type of orbital each lone pair is in
14. Draw Lewis structures for the following compounds. If they exhibit resonance, draw one other resonance structure for a total of two structures a. XeO,F2 b. NO, c. C,H, d. SO, e. SCI. f. KrF,
14. Draw Lewis structures for the following compounds. If they exhibit resonance, draw one other resonance structure for a total of two structures. b. NO a. ХеО,F, d. SO с. С.Н, f. KrF e. SCI, 15. Draw three resonance structures of NO, in which the atoms are arranged in the order NNO. Indicate the formal charges in each.
(i). Draw the structure of the products for the following reactions: (3.5 x 2 = 7 pts) NaHCO3 OOH Тон NaHCO3 (ii). Fill out the table below: (1.5 pt per box x 4 = 6 pts) Compounds Ionic/Polar/Non polar? Water Solubility? 0 OH Lotoon (iii). Name all the intermolecular forces of attraction present in the molecule below. (3 pts) (iv). Circle the most acidic protons in the following compounds: (2 x 2 = 4 pts)
Please solve and explain
1. (6 pts.) Rank the following compounds in order of increasing acidity. Each series should be considered separately. Use resonance and/or inductive effects to explain acidity. For full credit you will need to draw any resonance forms or indicate dipole if it is relevant. Also for each compound draw its conjugate base. Series 1: OH он OH O Series 2: CN 2. (4 pts.) Fill the reactions with the products and circle the favorite side: OH+...
Draw the structure of following compounds
3. Draw the structure of following compounds. 4-Bromo 3- chlorobenzoic acid 4-Chlorobutyl-3-chloro hexanoate Isobutyl acetate MacBook Air esc F1 F2 20 F $ 4 2 3 % 5 & 7 6 & Pentandjoic acid Cyclo propane dicarboxylic aad MacBook Air F2 F3 FS 97 # $
1. Draw all the significant resonance forms for the following structures, and indicate which are major and which are minor, or if you have two equally important forms, say so. The number of new forms you need to draw is shown in parentheses below the arrow. (a) N co 4. In each of the following reactions, indicate which structure is the nucleophile and which is the electrophile. Also draw the products (use the electron pair arrows to guide you). (a)...
1. Draw all resonance structures for the following compound.
Circle the major contributor (to the resonance hybrid) and give a
brief explanation for your choice. (4 pts) 2. Determine the
configuration (show priorities and work) for any chiral centers in
the molecule below. (2 pts)
2. Determine the configuration (show priorities and work) for
any chiral centers in the molecule below. (2 pts)
1. Draw all resonance structures for the following compound. Circle the major contributor (to the resonance hybrid)...
4. Resonance: (10 pts) Sketch the additional resonance forms of the given structure. Include charges, resonance arrows, and electron movement arrows. Circle the major resonance structure. If all structures are equivalent write 'same'. H. ΘΗ 4
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