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I’m
not sure what to do for the shirt synthesis so if someone could
help that...
4. 1) LIAIH 2) H20 5. Propose an efficient synthesis for one of the following transformations....
4. 1) LIAIH 2) H20 5. Propose an efficient synthesis for one of the following transformations. Please circle the synthesis you are completing. More than one step will be required; be sure to number each step. It will be significantly easier to award partial credit if you show the intermediate product after each step. CN Br ОН OR OH + enantiomer
can someone do these for me please! i’m having a hard time doing it the skill...
can
someone do these for me please! i’m having a hard time doing it
the skill 20.8 Draw a plausible mechanism for each of the following transformations MoO OM H501 MOH -HO гое dh skill 20.9 Draw a plausible mechanism for each of the following reactions 20.10 Predict the product of each of the following reactions H.S01 есен мон HO CONCEPTUAL CHECKPOINT 20.11 Propose a n t synthesis for each of the following transformations con 2.12 roser more 20.12 Predict...
can someone do these for me please! i’m having a hard time doing it the skill...
can
someone do these for me please! i’m having a hard time doing it
the skill 20.8 Draw a plausible mechanism for each of the following transformations MoO OM H501 MOH -HO гое dh skill 20.9 Draw a plausible mechanism for each of the following reactions 20.10 Predict the product of each of the following reactions H.S01 есен мон HO CONCEPTUAL CHECKPOINT 20.11 Propose a n t synthesis for each of the following transformations con 2.12 roser more 20.12 Predict...
chemistry please help 16. (a) (6 points) Show how to accomplish the following synthesis. mia Eto...
chemistry please help
16. (a) (6 points) Show how to accomplish the following synthesis. mia Eto OET ОН (b) (4 points) Propose an efficient synthesis for the following transformation. Br
For each of the reactions, show the reafents that would best accomplish the given synthesis, according...
For
each of the reactions, show the reafents that would best accomplish
the given synthesis, according to reactions we have atudied in
class. be sure to number your steps.
(a) CH3 ? CH3 "ОН (b) ? CH3CH2-CEC-CH2CH3 H CH2CH3 C=C H3CH2C H ? (CH3)2CHCH2C=CH o (CH3)2CHCH2CCH3 Br ? + enantiomer ( e) -CEC-H CEC (1) Hint: this is a multistep synthesis. Propose a series of reactions that would achieve the following transformation. Make sure to number the steps. . ?
Could someone please explain how to do this. Thank you. If you could explain in detail...
Could someone please explain how to do this. Thank you.
If you could explain in detail so I could understand I would
appreciate it very much!
Provide curved arrows to indicate the mechanism involved in each step of the following Hantzsch pyridine synthesis. 0 OH OH OH 0 он о O HO NH3 OH O H2N он он OH H
Not really sure how to solve this problem. The steps to do so would be greatly...
Not really sure how to solve this problem.
The steps to do so would be greatly appreciated. Thank you in
advance.
11. Consider a circuit of two capacitors, C and C2, in series. Prove that the equivalent capacitance of the circuit is
^ the top has been answered already Consider the following reaction: OH Н4С H,SO CH3 +...
^ the top has been answered already
Consider the following reaction: OH Н4С H,SO CH3 + ОН A Show the complete mechanism for the following transformations. Make sure to show all arrows depicting the movement of electrons. The above reaction (using acid and heat) causes a number of unwanted side products to form (a big mess). Propose a better synthesis for the product using the same starting materials. Show the reagents and intermediate steps to complete the synthesis: ОН. HzC...
I’ve tried a few and I’m not sure if I am right. Please complete questions 4...
I’ve tried a few and I’m not sure if I am right. Please
complete questions 4 and 5. PLEASE write clearly. Thank you so
much!
Give suitable reagents for each of the following conversions: 4. он OH OH (b) O2 (ii) H30 он Give suitable starting materials and reagents for the synthesis of each product shown. You may use any valid reagent (with any no. of carbons). он но NH2 он
if someone could help with this problem it would be greatly appreciated! 1 2 1 A...
if someone could help with this problem it would be
greatly appreciated!
1 2 1 A = 4 1 1 1 ? 4 dt 2 x'Ax, what are if there is no forcing on the system so the values of x after dt time... (use the forward Euler Method)
1 2 1 A = 4 1 1 1 ? 4 dt 2 x'Ax, what are if there is no forcing on the system so the values of x after dt...
4. 1) LIAIH 2) H20 5. Propose an efficient synthesis for one of the following transformations. Please circle the synthesis you are completing. More than one step will be required; be sure to number each step. It will be significantly easier to award partial credit if you show the intermediate product after each step. CN Br ОН OR OH + enantiomer
can
someone do these for me please! i’m having a hard time doing it
the skill 20.8 Draw a plausible mechanism for each of the following transformations MoO OM H501 MOH -HO гое dh skill 20.9 Draw a plausible mechanism for each of the following reactions 20.10 Predict the product of each of the following reactions H.S01 есен мон HO CONCEPTUAL CHECKPOINT 20.11 Propose a n t synthesis for each of the following transformations con 2.12 roser more 20.12 Predict...
can
someone do these for me please! i’m having a hard time doing it
the skill 20.8 Draw a plausible mechanism for each of the following transformations MoO OM H501 MOH -HO гое dh skill 20.9 Draw a plausible mechanism for each of the following reactions 20.10 Predict the product of each of the following reactions H.S01 есен мон HO CONCEPTUAL CHECKPOINT 20.11 Propose a n t synthesis for each of the following transformations con 2.12 roser more 20.12 Predict...
chemistry please help
16. (a) (6 points) Show how to accomplish the following synthesis. mia Eto OET ОН (b) (4 points) Propose an efficient synthesis for the following transformation. Br
For
each of the reactions, show the reafents that would best accomplish
the given synthesis, according to reactions we have atudied in
class. be sure to number your steps.
(a) CH3 ? CH3 "ОН (b) ? CH3CH2-CEC-CH2CH3 H CH2CH3 C=C H3CH2C H ? (CH3)2CHCH2C=CH o (CH3)2CHCH2CCH3 Br ? + enantiomer ( e) -CEC-H CEC (1) Hint: this is a multistep synthesis. Propose a series of reactions that would achieve the following transformation. Make sure to number the steps. . ?
Could someone please explain how to do this. Thank you.
If you could explain in detail so I could understand I would
appreciate it very much!
Provide curved arrows to indicate the mechanism involved in each step of the following Hantzsch pyridine synthesis. 0 OH OH OH 0 он о O HO NH3 OH O H2N он он OH H
Not really sure how to solve this problem.
The steps to do so would be greatly appreciated. Thank you in
advance.
11. Consider a circuit of two capacitors, C and C2, in series. Prove that the equivalent capacitance of the circuit is
^ the top has been answered already
Consider the following reaction: OH Н4С H,SO CH3 + ОН A Show the complete mechanism for the following transformations. Make sure to show all arrows depicting the movement of electrons. The above reaction (using acid and heat) causes a number of unwanted side products to form (a big mess). Propose a better synthesis for the product using the same starting materials. Show the reagents and intermediate steps to complete the synthesis: ОН. HzC...
I’ve tried a few and I’m not sure if I am right. Please
complete questions 4 and 5. PLEASE write clearly. Thank you so
much!
Give suitable reagents for each of the following conversions: 4. он OH OH (b) O2 (ii) H30 он Give suitable starting materials and reagents for the synthesis of each product shown. You may use any valid reagent (with any no. of carbons). он но NH2 он
if someone could help with this problem it would be
greatly appreciated!
1 2 1 A = 4 1 1 1 ? 4 dt 2 x'Ax, what are if there is no forcing on the system so the values of x after dt time... (use the forward Euler Method)
1 2 1 A = 4 1 1 1 ? 4 dt 2 x'Ax, what are if there is no forcing on the system so the values of x after dt...
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