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of the nucleophilic centers in the following compound. Fill numbers from left...
Skill Building Exercise: MO basis of nucleophiles and electrophiles/ Problem 1 Show all of the nucleophilic...
Skill Building Exercise: MO basis of nucleophiles and electrophiles/ Problem 1 Show all of the nucleophilic centers in the following compound. Fill numbers from left to right, from up to down Use only as many numbers as needed to identify the centers, starting with the number 1 1 2 3 10) 1112) Skill Building Exercise: MO basis of nucleophiles and electrophiles/ Problem 2 Show all of the nucleophilic centers in the following compound. Fill numbers from left to right, from...
OCH3 3. Indicate the electrophilic or nucleophilic centers for the following compounds: a) b) d) 4. Answer the foll...
OCH3 3. Indicate the electrophilic or nucleophilic centers for the following compounds: a) b) d) 4. Answer the following questions regarding 2,3-dimethylbutane: a) draw any staggered Newman projection of this compound looking down the C2-C3 bond. b) draw the highest energy conformation (as a Newman projection). Label each example of steric and/or torsional strain. c) draw the lowest energy conformation. Identify any sources of steric or torsional strain if present. m md iminetahm 5 Draw tra possiblechair conformatex For Jbrom-s-7ethiTmethychayo...
please show work Question 5 (4) Fill in any numbers as missing payoffs such that the...
please show work
Question 5 (4) Fill in any numbers as missing payoffs such that the game below is a game of Chicken Player 2 LEFT RIGHT Player 1 UP 10,10 DOWN 0,0 Question 6 (6) Assume a firm has a monopoly on its industry. For each of the outcome measures listed below, rank from Highest to Lowest: Uniform Pricing, 1t degree (perfect) price discrimination, 3rd degree price discrimination. [You may call them "Uniform price," "1"t degree," and "3d degree"]...
1. Fill in the blanks in the following equation. 2. Add up the mass numbers on...
1. Fill in the blanks in the following equation.
2. Add up the mass numbers on the right side of the above
equation. How does the sum compare to the mass number of uranium on
the left?
3. Add up the atomic numbers on the right side of the above
equation. How does the sum compare to the atomic number of uranium
on the left?
4. If a neutron transforms to a proton, what happens to the
number of neutrons...
In a series of numbers, a "mini peak" is a set of 3 numbers where the...
In a series of numbers, a "mini peak" is a set of 3 numbers where the middle number is strictly greater than its adjacent left and right neighbors. For example, the array: [ 4, 6, 2, 1 ] contains 1 mini peak, with 6 in the middle ([ 4, 6, 2]). Write full and complete C++ program to open a text file named numbers.txt in the working folder, which contains groups of numbers, one per line, with each group starting...
Hoyo 11. How many chirality centers are present in the compound at right (Write your answer on the line ar left). A...
Hoyo 11. How many chirality centers are present in the compound at right (Write your answer on the line ar left). A 12. Classify the absolute configuration for the compound below as either Ror S.. 0 0 HNK HY a R- (b) S- 0= N A /13. Classify the following alkene as either E-or Z-: A OCH +3 CH Br (a) E (b) z
3. Show the steps necessary to transform the acid on the left into the compound on...
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) CH2COH Cl b) Cl 4. Number these in order of ease of hydrolysis. 1 -easiest to hydrolyze, 4- hardest to hydrolyze. EN Cl
could you all please show the answers to number 3, and show the answer and explain for number 5? answer to number 4 i...
could you all please show the answers to number 3, and show the
answer and explain for number 5? answer to number 4 is not
needed.
please also draw out the spectrums for number 5.
3. What is the ratio of the protons for the following compounds (from left to right)? Provide multiplicity (splitting) for each proton. Provide number of different (symmetrically inequivalent) carbons for each compound. 3:2:3 Which compounds should have diastereotopic hydrogens? More than one correct answer is...
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions:...
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
2. Show the step(s) necessary to transform the compound on the left into the acid on...
2. Show the step(s) necessary to transform the compound on the left into the acid on the right. HOCH CH CH Br + HOCH2CH2CH,COH 19 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) H2C=CHCH_COH – H.C-chch_Coch; H2C=CHCH COH H2C=CHCHÖNCHS CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. CH;CH&CI CH,CHUCNHC,H, NCCH, CHOCCH,
Skill Building Exercise: MO basis of nucleophiles and electrophiles/ Problem 1 Show all of the nucleophilic centers in the following compound. Fill numbers from left to right, from up to down Use only as many numbers as needed to identify the centers, starting with the number 1 1 2 3 10) 1112) Skill Building Exercise: MO basis of nucleophiles and electrophiles/ Problem 2 Show all of the nucleophilic centers in the following compound. Fill numbers from left to right, from...
OCH3 3. Indicate the electrophilic or nucleophilic centers for the following compounds: a) b) d) 4. Answer the following questions regarding 2,3-dimethylbutane: a) draw any staggered Newman projection of this compound looking down the C2-C3 bond. b) draw the highest energy conformation (as a Newman projection). Label each example of steric and/or torsional strain. c) draw the lowest energy conformation. Identify any sources of steric or torsional strain if present. m md iminetahm 5 Draw tra possiblechair conformatex For Jbrom-s-7ethiTmethychayo...
please show work
Question 5 (4) Fill in any numbers as missing payoffs such that the game below is a game of Chicken Player 2 LEFT RIGHT Player 1 UP 10,10 DOWN 0,0 Question 6 (6) Assume a firm has a monopoly on its industry. For each of the outcome measures listed below, rank from Highest to Lowest: Uniform Pricing, 1t degree (perfect) price discrimination, 3rd degree price discrimination. [You may call them "Uniform price," "1"t degree," and "3d degree"]...
1. Fill in the blanks in the following equation.
2. Add up the mass numbers on the right side of the above
equation. How does the sum compare to the mass number of uranium on
the left?
3. Add up the atomic numbers on the right side of the above
equation. How does the sum compare to the atomic number of uranium
on the left?
4. If a neutron transforms to a proton, what happens to the
number of neutrons...
Hoyo 11. How many chirality centers are present in the compound at right (Write your answer on the line ar left). A 12. Classify the absolute configuration for the compound below as either Ror S.. 0 0 HNK HY a R- (b) S- 0= N A /13. Classify the following alkene as either E-or Z-: A OCH +3 CH Br (a) E (b) z
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) CH2COH Cl b) Cl 4. Number these in order of ease of hydrolysis. 1 -easiest to hydrolyze, 4- hardest to hydrolyze. EN Cl
could you all please show the answers to number 3, and show the
answer and explain for number 5? answer to number 4 is not
needed.
please also draw out the spectrums for number 5.
3. What is the ratio of the protons for the following compounds (from left to right)? Provide multiplicity (splitting) for each proton. Provide number of different (symmetrically inequivalent) carbons for each compound. 3:2:3 Which compounds should have diastereotopic hydrogens? More than one correct answer is...
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
2. Show the step(s) necessary to transform the compound on the left into the acid on the right. HOCH CH CH Br + HOCH2CH2CH,COH 19 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) H2C=CHCH_COH – H.C-chch_Coch; H2C=CHCH COH H2C=CHCHÖNCHS CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. CH;CH&CI CH,CHUCNHC,H, NCCH, CHOCCH,
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