I would like to know the mechanism of this reaction. Thank you in advance.
Disregard the structures above the reagents.
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I would like to know the mechanism of this reaction. Thank you
in advance.
Disregard the...
What's the mechanism of this reaction? HOA VOE- Ph Br 1) NaN3 2) H2, Pd-C ELUL...
What's the mechanism of this reaction?
HOA VOE- Ph Br 1) NaN3 2) H2, Pd-C ELUL CH3 3) 2 eq. CH20, 2 eq. NaBH3CN 4) H2O2 5) heat
10. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent...
10. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B, followed by C, and then D, your answer would be: ABCD. ? 'H Nang H2 1. LIAIH4 PCC OH HO Pd-C 2. H20 H* A B с D E...
Can someone explain in words how this mechanism works? I would just like to understand the...
Can someone explain in words how this mechanism works? I would
just like to understand the problems better. Thank you!
for example: I dont understand where the oxygen molecule
"disappears" to in the first reaction
1) show how the secondary amine can be I prepared by a successive reductive aminations: ammonium D AHS Dit H /Pd -NH2 Ha/ed ܬܕܢ ܓܓܢܬ
Starting with the alkane (butane), please work the mechanism to get the final, aldehyde product. Please...
Starting with the alkane (butane), please work
the mechanism to get the final, aldehyde product.
Please DRAW OUT the detailed mechanism and show ALL
ELECTRONS on the reagents and the reactants along with the arrows
pointing to the exact atom the electron(s) are being transferred
to.
Thank you SO MUCH in advance.
I just really want to understand the
mechanisms how the reagents rearrange the molecules via electron
pushing.
0 OH butyraldehyde 1-butanol DMP NaOH Br Br 1-bromobut-2-ene 1-bromobutane H2/Pd,...
I need some help with these please? Thank you so much in Advance! Review View E2...
I need some help with these please? Thank you so much in
Advance!
Review View E2 + 1 AaBbccde Albcendee AaBbCD AaBbCeDde 2) Draw line bond structures for the reagents you would need to make the following compounds by a Grignard Synthesis involving the indicated reagents. Ketone + Grignard Reagent Ester + Grignard Reagent Aldehyde + Grignard Reagent Epoxide + Grignard Reagent
Hello, can you please help me out with these problems. Thanks in advance. What reagents and...
Hello, can you please help me out with these problems. Thanks in
advance.
What reagents and conditions produce this transformation? 58. OH steps (A) 1. H2, Pd/C 3. NaOH, H2CO 4. NaBH4, CH3OH 5. Нзо", (CH3)2CO (B) 1. H2, Pd/C 2. NaBH4, CH OH 3. NaOH, Н.СО 4. pyridine-HCICrOs (PCC) 5. Нзо", (CH3)2CO (C) 1·Hao", (CH3)2CO 2. H Cros, H2S04, H2O 3. CH3MgBr 4. CHsCoH So2Cl (TsCl) 5. H2, Pd/C (D) 1. 1,3-butadiene, heat 2. H2, Pd/C 3. SOC12, pyridine...
Answer questions A-D please. ONLY ANSWER THE QUESTIONS IF YOU KNOW IT FOR SURE BECAUSE MY...
Answer questions A-D please. ONLY ANSWER THE QUESTIONS
IF YOU KNOW IT FOR SURE BECAUSE MY MONEY IS BEING WASTED WHEN MY
QUESTIONS ARE BEING ANSWERED WRONG. Thank you!!!
A.) Below is a summary of alkene reactions. Complete
them by providing the missing structures (including stereochemistry
wherever it applies).
B.) Draw the structure of the carbocation formed
during the reaction of the alkene from chart A with HCl.
C.) Draw the mechanism of the reaction of Br2 addition.
D.) Draw...
I know the correct answer is C but I would like some explanation thank you! onside...
I know the correct answer is C but I would like some
explanation thank you!
onside In an experiment in whichM 0.10 M, the initial rate was found to be R M/s. With r the reaction: X + 2Y Z rate k[XM which of the following initial concentrations will the rate double to 2R M/s? A) [X O.10 M, [M -0.40 M B) X 0.20 M, Y 0.20 M ) [X] = 0.40 M, [Y] =0.05 M- "D) [X] =...
Which reagents would you use to convert the aldehyde to the alcohol shown? Thank You!! Which reagents would you use to...
Which reagents would you use to convert the aldehyde to the
alcohol shown? Thank You!!
Which reagents would you use to convert the aldehyde to the alcohol shown? H2. Pd/C NaBH4 in MeOH 1. CH3Li and H307 1. CH3Li in THF 2. H30+ 1. LIAIH4 2. H30+
Predict the products of the following reactions. I will rate fast. Thank you in advance! excess...
Predict the products of the following reactions.
I will rate fast. Thank you in advance!
excess NaNH2 THF Br Br H 1. NaNH2 2. CH3CH2Br H2SO4, H20 v MSO. MO H2, Pd/Baso quinoline, CH3OH Na, NH3 Na, NH, 1 equivalent HBr NaNH2 Br (excess) 1. Sia BH, THF 2. H202, NaOH h. HgSO4 H2SO4 H20
What's the mechanism of this reaction?
HOA VOE- Ph Br 1) NaN3 2) H2, Pd-C ELUL CH3 3) 2 eq. CH20, 2 eq. NaBH3CN 4) H2O2 5) heat
10. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B, followed by C, and then D, your answer would be: ABCD. ? 'H Nang H2 1. LIAIH4 PCC OH HO Pd-C 2. H20 H* A B с D E...
Can someone explain in words how this mechanism works? I would
just like to understand the problems better. Thank you!
for example: I dont understand where the oxygen molecule
"disappears" to in the first reaction
1) show how the secondary amine can be I prepared by a successive reductive aminations: ammonium D AHS Dit H /Pd -NH2 Ha/ed ܬܕܢ ܓܓܢܬ
Starting with the alkane (butane), please work
the mechanism to get the final, aldehyde product.
Please DRAW OUT the detailed mechanism and show ALL
ELECTRONS on the reagents and the reactants along with the arrows
pointing to the exact atom the electron(s) are being transferred
to.
Thank you SO MUCH in advance.
I just really want to understand the
mechanisms how the reagents rearrange the molecules via electron
pushing.
0 OH butyraldehyde 1-butanol DMP NaOH Br Br 1-bromobut-2-ene 1-bromobutane H2/Pd,...
I need some help with these please? Thank you so much in
Advance!
Review View E2 + 1 AaBbccde Albcendee AaBbCD AaBbCeDde 2) Draw line bond structures for the reagents you would need to make the following compounds by a Grignard Synthesis involving the indicated reagents. Ketone + Grignard Reagent Ester + Grignard Reagent Aldehyde + Grignard Reagent Epoxide + Grignard Reagent
Hello, can you please help me out with these problems. Thanks in
advance.
What reagents and conditions produce this transformation? 58. OH steps (A) 1. H2, Pd/C 3. NaOH, H2CO 4. NaBH4, CH3OH 5. Нзо", (CH3)2CO (B) 1. H2, Pd/C 2. NaBH4, CH OH 3. NaOH, Н.СО 4. pyridine-HCICrOs (PCC) 5. Нзо", (CH3)2CO (C) 1·Hao", (CH3)2CO 2. H Cros, H2S04, H2O 3. CH3MgBr 4. CHsCoH So2Cl (TsCl) 5. H2, Pd/C (D) 1. 1,3-butadiene, heat 2. H2, Pd/C 3. SOC12, pyridine...
Answer questions A-D please. ONLY ANSWER THE QUESTIONS
IF YOU KNOW IT FOR SURE BECAUSE MY MONEY IS BEING WASTED WHEN MY
QUESTIONS ARE BEING ANSWERED WRONG. Thank you!!!
A.) Below is a summary of alkene reactions. Complete
them by providing the missing structures (including stereochemistry
wherever it applies).
B.) Draw the structure of the carbocation formed
during the reaction of the alkene from chart A with HCl.
C.) Draw the mechanism of the reaction of Br2 addition.
D.) Draw...
I know the correct answer is C but I would like some
explanation thank you!
onside In an experiment in whichM 0.10 M, the initial rate was found to be R M/s. With r the reaction: X + 2Y Z rate k[XM which of the following initial concentrations will the rate double to 2R M/s? A) [X O.10 M, [M -0.40 M B) X 0.20 M, Y 0.20 M ) [X] = 0.40 M, [Y] =0.05 M- "D) [X] =...
Which reagents would you use to convert the aldehyde to the
alcohol shown? Thank You!!
Which reagents would you use to convert the aldehyde to the alcohol shown? H2. Pd/C NaBH4 in MeOH 1. CH3Li and H307 1. CH3Li in THF 2. H30+ 1. LIAIH4 2. H30+
Predict the products of the following reactions.
I will rate fast. Thank you in advance!
excess NaNH2 THF Br Br H 1. NaNH2 2. CH3CH2Br H2SO4, H20 v MSO. MO H2, Pd/Baso quinoline, CH3OH Na, NH3 Na, NH, 1 equivalent HBr NaNH2 Br (excess) 1. Sia BH, THF 2. H202, NaOH h. HgSO4 H2SO4 H20
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