A)When forming enolate, a ketone (ex: acetone) reacts with NaOH and acts like a nucleophile, how...
A)When forming enolate, a ketone (ex: acetone) reacts with NaOH and acts like a nucleophile, how is the negative charge stabilized? Please include drawn reaction, and clear explanation. Thank you
Homework Answers
Add Answer to:
A)When forming enolate, a ketone (ex: acetone) reacts with NaOH
and acts like a nucleophile, how...
A) In the process of forming an enolate, a ketone like acetone reacts with sodium hydroxide...
A) In the process of forming an enolate, a ketone like acetone reacts with sodium hydroxide and acts like a nucleophile, how is the negative charge stabilized? Must include drawn reaction. B) Given 100 cc of acetone that contains sodium hydroxide, and 10 cc of benzaldehyde, how much dibenzalacetone is produced, show calculations. Thank you!
A) In the process of forming an enolate, a ketone like acetone reacts with sodium hydroxide...
A) In the process of forming an enolate, a ketone like acetone reacts with sodium hydroxide and acts like a nucleophile, how is the negative charge stabilized? Draw the reaction. B) Given 100 cc of acetone that contains sodium hydroxide, and 10 cc of benzaldehyde, how much dibenzalacetone is produced, show calculations.
How can you tell if a reactant, like the NaOH, is a strong/weak nucleophile or base...
How can you tell if a reactant, like the NaOH, is a
strong/weak nucleophile or base to determine what mechanism you
use? The picture provided has the correct answers. I just don't
understand how to get to them.
3. Draw a structural formula for the major organic product(s) of each reaction and specify the mechanism by which each product is formed (SN1, S2, E, or E2). E2 NaOH Н,0 CH3CH2ONa CH3CH2OH E2 CH2ONa иис CH3OH OCH3 Br CH3OH ИИ E1...
please don't use any abbreviations! like I don't know how to draw anything like oet or...
please don't use any
abbreviations! like I don't know how to draw anything like oet or
an R group like please just draw out the whole thing!
NaOH ethanol HO This reaction involves an intramolecular Michael reaction followed by an intramolecular aldol reaction. The steps involved are as follows: 1. Deprotonation to form enolate ion 1; 2. Cyclization via an intramolecular Michael reaction to form intermediate 2; 3. Deprotonation to form enolate ion 3; 4. Intramolecular aldol cyclization to form...
how do i draw the enolate anion and the organic product in the third and fourth box? please include lone pair electrons...
how do i draw the enolate anion and the organic product in the
third and fourth box? please include lone pair electrons and formal
charges.
thank you.
Draw the curved arrow mechanism for the reaction between the aldehyde and propyl bromide, including the final product. Be sure to include nonzer formal charges and lone pair electrons on all appropriate atoms. 3rd attempt Il See Periodic Table See Hint Draw the resonance structure of the enolate lon. Do NOT draw curved...
8 2 H NaOH Еюн 5 benzaldehyde d 1.044 acetone d0.791 When doing part B of the reaction for lab, how many grams of b...
8 2 H NaOH Еюн 5 benzaldehyde d 1.044 acetone d0.791 When doing part B of the reaction for lab, how many grams of benzaldehyde (#4) would you need if you are trying to make a maximum theoretical yield of 15 grams of dibenzalacetone (#6)? Acetone: density 0.791 g/mL and molar mass 58.08 grams/mole Benzaldehyde: density 1.044 g/mL and molar mass 106.12 grams/mole Dibenzalacetone: molar mass = 234.29 grams/mole Enter answer.... со
When 100mL of 0.0125 M ascorbic acid is titrated with 0.010 M NaOH, how many equivalence points w...
When 100mL of 0.0125 M ascorbic acid is titrated with 0.010 M NaOH, how many equivalence points will the titration curve have, and what pH indicator(s) could be used? Please show process and explanation. Thank you!
Please provide step 1 and 2 STANDARD VIEW PRINEER VERSION Practice Problem 21.82 Nitriles undergo alkylation...
Please provide step 1 and 2
STANDARD VIEW PRINEER VERSION Practice Problem 21.82 Nitriles undergo alkylation at the a position much like ketones undergo alkylation at the a position BACK The a position of the nitrile is first deprotonated to give a resonance-stabilized anion (like an enolate), which then functions as a nucleophile to attack the alkyl halide. Dran the mechanism described above for the transformation below (propyl chloride will be the RX in this reaction). For the mechanism, draw...
when .0015 M of HCl reacts with .0035 M NaOH. how do I get HCl as...
when .0015 M of HCl reacts with .0035 M NaOH.
how do I get HCl as the limiting reactant?
HC # Results/Observations 1 Reaction Between Hydrochloric Acid and Sodium Hydroxide Table 1 ml LOM mol HCI ml 1.0M mol NaOH Temperature NaOHT change. "C 19. 10 0045 50L2012 .0005 22.4 #2 19.10.0 .004 10.09.11 .001 24.3 #3 1949350 -0035 15.020 Ốc DD15 265 #499 300 003 20.0 20.10 .002 27.3 #5 A5 2.0 .0025 25.0 20. 0 0025 2100 #6...
I need help with my chem lab report. I need to identify the unknown structure. Please...
I need help with my chem lab report.
I need to identify the unknown structure.
Please help me identify the importance of each peak in the
spectrums.
What would the reactions look like for this structure when it
reacts with ethanol for DNPH test, CrO3 and dioxane and NaOH for
iodoform test.
The compound was a clear liquid. It is insoluble in water. tests
positive for DNPH test, positive for CrO3 test and negative for
iodoform. These results tell me...
How can you tell if a reactant, like the NaOH, is a
strong/weak nucleophile or base to determine what mechanism you
use? The picture provided has the correct answers. I just don't
understand how to get to them.
3. Draw a structural formula for the major organic product(s) of each reaction and specify the mechanism by which each product is formed (SN1, S2, E, or E2). E2 NaOH Н,0 CH3CH2ONa CH3CH2OH E2 CH2ONa иис CH3OH OCH3 Br CH3OH ИИ E1...
please don't use any
abbreviations! like I don't know how to draw anything like oet or
an R group like please just draw out the whole thing!
NaOH ethanol HO This reaction involves an intramolecular Michael reaction followed by an intramolecular aldol reaction. The steps involved are as follows: 1. Deprotonation to form enolate ion 1; 2. Cyclization via an intramolecular Michael reaction to form intermediate 2; 3. Deprotonation to form enolate ion 3; 4. Intramolecular aldol cyclization to form...
how do i draw the enolate anion and the organic product in the
third and fourth box? please include lone pair electrons and formal
charges.
thank you.
Draw the curved arrow mechanism for the reaction between the aldehyde and propyl bromide, including the final product. Be sure to include nonzer formal charges and lone pair electrons on all appropriate atoms. 3rd attempt Il See Periodic Table See Hint Draw the resonance structure of the enolate lon. Do NOT draw curved...
8 2 H NaOH Еюн 5 benzaldehyde d 1.044 acetone d0.791 When doing part B of the reaction for lab, how many grams of benzaldehyde (#4) would you need if you are trying to make a maximum theoretical yield of 15 grams of dibenzalacetone (#6)? Acetone: density 0.791 g/mL and molar mass 58.08 grams/mole Benzaldehyde: density 1.044 g/mL and molar mass 106.12 grams/mole Dibenzalacetone: molar mass = 234.29 grams/mole Enter answer.... со
Please provide step 1 and 2
STANDARD VIEW PRINEER VERSION Practice Problem 21.82 Nitriles undergo alkylation at the a position much like ketones undergo alkylation at the a position BACK The a position of the nitrile is first deprotonated to give a resonance-stabilized anion (like an enolate), which then functions as a nucleophile to attack the alkyl halide. Dran the mechanism described above for the transformation below (propyl chloride will be the RX in this reaction). For the mechanism, draw...
when .0015 M of HCl reacts with .0035 M NaOH.
how do I get HCl as the limiting reactant?
HC # Results/Observations 1 Reaction Between Hydrochloric Acid and Sodium Hydroxide Table 1 ml LOM mol HCI ml 1.0M mol NaOH Temperature NaOHT change. "C 19. 10 0045 50L2012 .0005 22.4 #2 19.10.0 .004 10.09.11 .001 24.3 #3 1949350 -0035 15.020 Ốc DD15 265 #499 300 003 20.0 20.10 .002 27.3 #5 A5 2.0 .0025 25.0 20. 0 0025 2100 #6...
I need help with my chem lab report.
I need to identify the unknown structure.
Please help me identify the importance of each peak in the
spectrums.
What would the reactions look like for this structure when it
reacts with ethanol for DNPH test, CrO3 and dioxane and NaOH for
iodoform test.
The compound was a clear liquid. It is insoluble in water. tests
positive for DNPH test, positive for CrO3 test and negative for
iodoform. These results tell me...
Most questions answered within 3 hours.
-
The average length of time between arrivals at a turnpike
toll-booth is 26 seconds. What is...
asked 1 hour ago -
(a) A piston at 6.1 atm contains a gas that occupies a volume of
3.5 L....
asked 2 hours ago -
Please answer true or false. Words
cannot be changed or added in to make it true...
asked 2 hours ago -
An empty test tube weighs 15.923 grams. Then,
MgCl2•6H2O is added into the test tube. After...
asked 2 hours ago -
Assume memory access is 10 units of time and disk access is
10000 units of time....
asked 2 hours ago -
1. Are all good samples random?
2. Magazines often report surveys giving statistics such as “63%...
asked 3 hours ago -
Under all the various types of market structures, firms
must eventually earn some economic profits for...
asked 2 hours ago -
Consider the following fitness regime for a single locus trait
with two co-dominant alleles: w11 =...
asked 2 hours ago -
A large cable company reports the following.
80% of its customers subscribe to its cable TV...
asked 3 hours ago -
Please answer the question in brief.
Discuss the role of ERP in organizations. Are ERP tools...
asked 2 hours ago -
Discuss the pros and cons of collaborative software such
as SameTime. Does it increase productivity? What...
asked 3 hours ago -
Buying your in-laws a gift because it’s expected is
due to the ____________ motive of gift-giving....
asked 3 hours ago