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Chapter 6 [References) Question 5 o 1 pt CH3 CH3 OCH CH3 ÇI CH3 CI Cl2...
Chapter 6 [References) Question 15 1 pt CI CI Question 16 1 pt HCI H3C CH3...
Chapter 6 [References) Question 15 1 pt CI CI Question 16 1 pt HCI H3C CH3 HC Question 17 CH3 H3C CH3 1 pt Question 18 1 pt H2C CH3 CI Question 19 1 pt CH3 H2C CH3 CI Question 20 1 pt Question 21 ® 1 pt Treating 1,3-pentadiene with one mole of HCl give a mixture of five isomeric products. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism Question 22...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...
Chapter 6 Question 6 (References) 1 pt H Question 7 1 pt H Cl2 NaOH H...
Chapter 6 Question 6 (References) 1 pt H Question 7 1 pt H Cl2 NaOH H H NaCl H2O Question 8 Н X) 1 pt H Question 9 © 1 pt O Question 101 pt H Question 11 1 pt Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Question 12 1 pt Arrow-pushing Instructions Question 13 1 pt Question 14 1 pt nn Question 15 1 pt Question 16 1 pt :cis...
Question 1 1 pt (References) CH3 Question 2 1 pt Question 3 1 pt CH3 Question...
Question 1 1 pt (References) CH3 Question 2 1 pt Question 3 1 pt CH3 Question 4 1 pt CH Question 5 1 pt When isopropylidenecyclohexane is treated with strong acid at room temperature, isomerization occurs in two steps to yield 1- isopropyleyclohexene. One of these steps is shown below; add curved arrows to the mechanism to indicate the movement of electrons in this step. Question 6 1 pt Question 7 Arrow-pushing Instructions pt atid no XT other H-CI CH3...
Chapter 7 (References) Question 7 1 pt Question 8 1 pt 1. (sia) BH, THF,0°C 2....
Chapter 7 (References) Question 7 1 pt Question 8 1 pt 1. (sia) BH, THF,0°C 2. K2CO3, H2O2, H20 ? Question 9 1 pt Question 10 1 pt Question 11 1 pt Functional groups such as alkynes react the same in complex molecules as they do in simpler structures. Draw the expected product(s) for this reaction. Question 12 1 pt Question 13 1 pt • Use the wedge/hash bond tools to indicate stereochemistry where exists. • If the reaction produces...
I attached the table that was given. assignment- 80% References pt pr CH3 1 pt CH3CCH2CH3...
I attached the table that was given.
assignment- 80% References pt pr CH3 1 pt CH3CCH2CH3 CH3 CH3CHCH2CH3 + Cl2 + HCI Assuming that the reaction proceeds via a radical chain reaction mechanism, calculate All for the first propagation step of this reaction. J/mol This first step is In the box below, draw the structure of the species most closely resembling the transition state (ie, if the transition state resembles the products, draw the radical) . Include all valence lone...
Chapter 6 [References) Question 7 1 pt Br Question 8 1 pt CH2OH Question 9 1...
Chapter 6 [References) Question 7 1 pt Br Question 8 1 pt CH2OH Question 9 1 pt Br—Br Насот Question 10 1 pt Question 11 1 pt The mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilic attack leads to intermediate 2, which goes on to form the final product. In cases that involve a negatively charged nucleophile, the attack of the nucleophile leads directly to the product. Question 12 1 pt Question 13 % 1 pt You Hotel...
Chapter 7 [References) Question 1 1 pt ОН. Question 2 1 pt + CH3CH2C=CH CH3CHO CH3CH2C=C...
Chapter 7 [References) Question 1 1 pt ОН. Question 2 1 pt + CH3CH2C=CH CH3CHO CH3CH2C=C C-CH3 Н Question 3 1 pt 1-Butyne Acetaldehyde Question 4 1 pt Question 5 1 pt Question 6 1 pt Alkyne anions react with the carbonyl groups of aldehydes and ketones to form alkynyl alcohols. The reaction mechanism between 1-butyne and acetaldehyde includes the following steps: 1. Sodium amide deprotonates the terminal alkyne; 2. The alkyne anion acts as a nucleophile and adds to...
Question 14 1 pts Which of the following compounds contains an ether functional group? CH3-CH2-O-CH2-CH, OCH-O-H...
Question 14 1 pts Which of the following compounds contains an ether functional group? CH3-CH2-O-CH2-CH, OCH-O-H o CH3-CH2-C.CH co CH3-CH CH CH3-C OH CH₃ D Question 15 1 pts acer
What is the major product of the reaction below? 1) BHY-THF 2) H2O2, NaOH Select one:...
What is the major product of the reaction below? 1) BHY-THF 2) H2O2, NaOH Select one: OH a. OH ob. OH OH d. Which is the most stable conformation of butane? Select one: CH3 H H a. H CH3 H Сна H. CH3 b. H I I- CH3 CH I C. H H CH3 Question 21 Not yet answered Marked out of 3.00 p Flag question What is the IUPAC name of the molecule shown below HO Br Select one:...
Chapter 6 [References) Question 15 1 pt CI CI Question 16 1 pt HCI H3C CH3 HC Question 17 CH3 H3C CH3 1 pt Question 18 1 pt H2C CH3 CI Question 19 1 pt CH3 H2C CH3 CI Question 20 1 pt Question 21 ® 1 pt Treating 1,3-pentadiene with one mole of HCl give a mixture of five isomeric products. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism Question 22...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...
Chapter 6 Question 6 (References) 1 pt H Question 7 1 pt H Cl2 NaOH H H NaCl H2O Question 8 Н X) 1 pt H Question 9 © 1 pt O Question 101 pt H Question 11 1 pt Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Question 12 1 pt Arrow-pushing Instructions Question 13 1 pt Question 14 1 pt nn Question 15 1 pt Question 16 1 pt :cis...
Question 1 1 pt (References) CH3 Question 2 1 pt Question 3 1 pt CH3 Question 4 1 pt CH Question 5 1 pt When isopropylidenecyclohexane is treated with strong acid at room temperature, isomerization occurs in two steps to yield 1- isopropyleyclohexene. One of these steps is shown below; add curved arrows to the mechanism to indicate the movement of electrons in this step. Question 6 1 pt Question 7 Arrow-pushing Instructions pt atid no XT other H-CI CH3...
Chapter 7 (References) Question 7 1 pt Question 8 1 pt 1. (sia) BH, THF,0°C 2. K2CO3, H2O2, H20 ? Question 9 1 pt Question 10 1 pt Question 11 1 pt Functional groups such as alkynes react the same in complex molecules as they do in simpler structures. Draw the expected product(s) for this reaction. Question 12 1 pt Question 13 1 pt • Use the wedge/hash bond tools to indicate stereochemistry where exists. • If the reaction produces...
I attached the table that was given.
assignment- 80% References pt pr CH3 1 pt CH3CCH2CH3 CH3 CH3CHCH2CH3 + Cl2 + HCI Assuming that the reaction proceeds via a radical chain reaction mechanism, calculate All for the first propagation step of this reaction. J/mol This first step is In the box below, draw the structure of the species most closely resembling the transition state (ie, if the transition state resembles the products, draw the radical) . Include all valence lone...
Chapter 6 [References) Question 7 1 pt Br Question 8 1 pt CH2OH Question 9 1 pt Br—Br Насот Question 10 1 pt Question 11 1 pt The mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilic attack leads to intermediate 2, which goes on to form the final product. In cases that involve a negatively charged nucleophile, the attack of the nucleophile leads directly to the product. Question 12 1 pt Question 13 % 1 pt You Hotel...
Chapter 7 [References) Question 1 1 pt ОН. Question 2 1 pt + CH3CH2C=CH CH3CHO CH3CH2C=C C-CH3 Н Question 3 1 pt 1-Butyne Acetaldehyde Question 4 1 pt Question 5 1 pt Question 6 1 pt Alkyne anions react with the carbonyl groups of aldehydes and ketones to form alkynyl alcohols. The reaction mechanism between 1-butyne and acetaldehyde includes the following steps: 1. Sodium amide deprotonates the terminal alkyne; 2. The alkyne anion acts as a nucleophile and adds to...
Question 14 1 pts Which of the following compounds contains an ether functional group? CH3-CH2-O-CH2-CH, OCH-O-H o CH3-CH2-C.CH co CH3-CH CH CH3-C OH CH₃ D Question 15 1 pts acer
What is the major product of the reaction below? 1) BHY-THF 2) H2O2, NaOH Select one: OH a. OH ob. OH OH d. Which is the most stable conformation of butane? Select one: CH3 H H a. H CH3 H Сна H. CH3 b. H I I- CH3 CH I C. H H CH3 Question 21 Not yet answered Marked out of 3.00 p Flag question What is the IUPAC name of the molecule shown below HO Br Select one:...
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