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Please answer this question according to the instruction, Thank
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6. (16 pt) Use...
Please show all work for Number 5: CH3OH and number 3, HF one. Thank you Complete...
Please show all work for
Number 5: CH3OH and number 3, HF one. Thank you
Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
provide a detailed, arrow pushing, step-by-step reaction mechanism for the following: Please be legible. Thank you...
provide a detailed, arrow pushing, step-by-step reaction
mechanism for the following:
Please be legible. Thank you so much!
3. Provide a detailed, arrow-pushing, step-by-step reaction mechanism for the following. OH *
Could you please show the full mechanism for this reaction with arrow pushing. Thank you so...
Could you please show the full mechanism for this reaction with
arrow pushing. Thank you so much!
OS 88 N-Br 064-0 NaOH H2O Br Racemic mixture Scheme 1: Formation of epxoycyclohexane starting with cyclohexene.
PLEASE ANSWER ALL A-G, will give thumbs up!! FOR A, just need explanation why reaction occurs...
PLEASE ANSWER ALL A-G, will
give thumbs up!! FOR A, just need explanation why reaction occurs
at C2 position rather than C3, already have mechanism drawn...
PLEASE EXPLAIN OR AT LEAST
JUST ANSWER ALL ASAP, BEFORE TOMORROW!!
10. Furan, an aromatic heterocycle, is capable of undergoing electrophilic aromatic substitution. When furan is treated with an acid chloride in the presence of a Lewis acid, Friedel-Crafts acylation occurs in which the electrophile is installed exclusively at the C2 position. Provide...
Can you please explain to me what I did wrong with my resonance structures and then...
Can you please explain to me
what I did wrong with my resonance structures and then show me how
I should have drawn them? Thank you.
5. (24 points) Draw reasonable resonance structures. You must use electron-pushing arrow notation to show the conversion of a resonance structure into another resonance structure for full credit. a. Draw 3 additionalreasonable resonance structures: ཡི – ཨར་ང – ། དེ་ s དང་ ས་ ལ་ EW=c k=
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...
7-9 please! 4 7. One of the following is much more acidic than the other. Circle...
7-9 please!
4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
show all work please thank you!!! 3. (10 pts total) Consider the following alkene addition reaction:...
show all work please thank you!!!
3. (10 pts total) Consider the following alkene addition reaction: Brz H2O НО Br a. (3 pts) This type of alkene addition reaction is mediated by both Lewis acids and bases. Of the two inorganic reactants (Br2 and H2O), place a triangle (1) around the one which functions as a Lewis acid in the above transformation b. (3 pts) of the two regioisomeric reaction products shown, only one is observed to form under the...
please help me with both questions, thank you so much!! Question 17 Predict the product for...
please help me with both questions, thank you so much!!
Question 17 Predict the product for the following reaction. 1. DIBAH 2. H,0 | ОН ОН ОН Оооо Question 16 Predict the product for the following reaction. 1. SOCI/pyridine 2. LiAl[OC(CH3)3]H OCH3 SOCI soci II iv 0 0 0 0 0
Please type the answer for i can copy it. Thank you very much. -Question Describe decision...
Please type the answer for i can copy it. Thank you very much. -Question Describe decision processing control structures. Provide a unique scenario that requires the use of decision processing to solve a business problem.
Please show all work for
Number 5: CH3OH and number 3, HF one. Thank you
Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
provide a detailed, arrow pushing, step-by-step reaction
mechanism for the following:
Please be legible. Thank you so much!
3. Provide a detailed, arrow-pushing, step-by-step reaction mechanism for the following. OH *
Could you please show the full mechanism for this reaction with
arrow pushing. Thank you so much!
OS 88 N-Br 064-0 NaOH H2O Br Racemic mixture Scheme 1: Formation of epxoycyclohexane starting with cyclohexene.
PLEASE ANSWER ALL A-G, will
give thumbs up!! FOR A, just need explanation why reaction occurs
at C2 position rather than C3, already have mechanism drawn...
PLEASE EXPLAIN OR AT LEAST
JUST ANSWER ALL ASAP, BEFORE TOMORROW!!
10. Furan, an aromatic heterocycle, is capable of undergoing electrophilic aromatic substitution. When furan is treated with an acid chloride in the presence of a Lewis acid, Friedel-Crafts acylation occurs in which the electrophile is installed exclusively at the C2 position. Provide...
Can you please explain to me
what I did wrong with my resonance structures and then show me how
I should have drawn them? Thank you.
5. (24 points) Draw reasonable resonance structures. You must use electron-pushing arrow notation to show the conversion of a resonance structure into another resonance structure for full credit. a. Draw 3 additionalreasonable resonance structures: ཡི – ཨར་ང – ། དེ་ s དང་ ས་ ལ་ EW=c k=
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...
7-9 please!
4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
show all work please thank you!!!
3. (10 pts total) Consider the following alkene addition reaction: Brz H2O НО Br a. (3 pts) This type of alkene addition reaction is mediated by both Lewis acids and bases. Of the two inorganic reactants (Br2 and H2O), place a triangle (1) around the one which functions as a Lewis acid in the above transformation b. (3 pts) of the two regioisomeric reaction products shown, only one is observed to form under the...
please help me with both questions, thank you so much!!
Question 17 Predict the product for the following reaction. 1. DIBAH 2. H,0 | ОН ОН ОН Оооо Question 16 Predict the product for the following reaction. 1. SOCI/pyridine 2. LiAl[OC(CH3)3]H OCH3 SOCI soci II iv 0 0 0 0 0
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