Provide a stepwise mechanism for the formation of
2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from
3,4-dimethoxybenzaldehyde and 1-indanone. Please show all steps!
This is a crossed aldol condensation. Thanks!Homework Answers
Add Answer to:
Provide a stepwise mechanism for the formation of
2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from
3,4-dimethoxybenzaldehyde and 1-indanone. Please show all...
the top half of the image depicts the synthesis of 2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from 1-indanone and 3,4-dimethoxybenzaldehyde. The...
the top half of the image depicts the synthesis of
2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from
1-indanone and 3,4-dimethoxybenzaldehyde. The bottom half of the
image attached shows the table of chemicals used in the reaction.
How would I calculate theoretical yield and furthermore, the
percent yield? This experiment had a lot of chemicals used and I
don't know where to start.
Crossed aldol condensation of 3.4-dimethoxybenzaldehyde and l-indanone your co m ments cholateOH -4.0 dehydration formation OH O CHOY carbonyl addition initial aldol product...
Product was formed successfully based on the exp. below (about 85% yield), please interpret/discuss HNMR/IR in...
Product was formed successfully based on the exp. below (about
85% yield), please interpret/discuss HNMR/IR in as much detail as
possible and assign peaks on HNMR (which peak represents which
protons of which group, etc). Note: I already know how you
determine the formation of the product so you can skip that part of
part b).
Based on this exp:
Discuss the IR spectrum and what is the peak in IR that you can see for a specific functional group...
HW 22: Enolates 1. Provide a detailed, stepwise mechanism for the base-catalyzed enolization (keto enol tautomerism) of acetaldehyde. 2. Provide the major organic product of the folowing reactio...
HW 22: Enolates 1. Provide a detailed, stepwise mechanism for the base-catalyzed enolization (keto enol tautomerism) of acetaldehyde. 2. Provide the major organic product of the folowing reaction. 3. Provide the major organic product of the following reaction LDA 4. Which of the following ketones will give a positive iodoform test? A) 4-heptanone D) cyclohexanone B) 3-hexanone C)2-hexanone 5. Provide the major organic product of the following reaction. 6. Provide the structure of the major organic product which results when...
the top half of the image depicts the synthesis of
2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from
1-indanone and 3,4-dimethoxybenzaldehyde. The bottom half of the
image attached shows the table of chemicals used in the reaction.
How would I calculate theoretical yield and furthermore, the
percent yield? This experiment had a lot of chemicals used and I
don't know where to start.
Crossed aldol condensation of 3.4-dimethoxybenzaldehyde and l-indanone your co m ments cholateOH -4.0 dehydration formation OH O CHOY carbonyl addition initial aldol product...
Product was formed successfully based on the exp. below (about
85% yield), please interpret/discuss HNMR/IR in as much detail as
possible and assign peaks on HNMR (which peak represents which
protons of which group, etc). Note: I already know how you
determine the formation of the product so you can skip that part of
part b).
Based on this exp:
Discuss the IR spectrum and what is the peak in IR that you can see for a specific functional group...
HW 22: Enolates 1. Provide a detailed, stepwise mechanism for the base-catalyzed enolization (keto enol tautomerism) of acetaldehyde. 2. Provide the major organic product of the folowing reaction. 3. Provide the major organic product of the following reaction LDA 4. Which of the following ketones will give a positive iodoform test? A) 4-heptanone D) cyclohexanone B) 3-hexanone C)2-hexanone 5. Provide the major organic product of the following reaction. 6. Provide the structure of the major organic product which results when...
Most questions answered within 3 hours.
-
What volume of a 0.251 M perchloric
acid solution is required to neutralize
14.6 mL of...
asked 45 seconds from now -
Amplitude=3;
fs=8000;
n=0:399;
t=0:1/fs: n*1/fs-1/fs;
signal=3+3*cos(2*pi*1100*t)+3*cos(2*pi*2200*t)+3*cos(2*pi*3300*t);
fftSignal= fft(signal);
fftSignal=f ftshift (fftSignal);
f=fs/2*linspace(-1,1,fs);
plot(f,abs(fftsignal);
xlabel('Frequency(Hz)’)
yla
asked 23 seconds ago -
Write a method called removeDuplicates that
accepts a PriorityQueue of integers as a parameter
and modifies...
asked 2 minutes ago -
What is the wavelength, in cm, of a microwave having a frequency
of 3.44 x 10^9...
asked 20 minutes ago -
A new business venture must develop a comprehensive business
plan to borrow money to get started....
asked 22 minutes ago -
Madtack Company uses a job-order costing system and started the month
of March with only one...
asked 24 minutes ago -
Describe how to distinguish true motility from brownian motion
and fluid flow when viewing a wet...
asked 27 minutes ago -
A manufacturer of game controllers is concerned that its
controller may be difficult for left-handed users....
asked 29 minutes ago -
Water at gauge pressure of 3.8 atmospheres at street level
enters an office building at 0.60...
asked 43 minutes ago -
Quick question, I want to know how to convert decimal numbers to
binary number, when i...
asked 1 hour ago -
You found out that now you are going to receive payments of
$8,500 for the next...
asked 1 hour ago -
17.
Technician A says that leaking components are usually repaired
rather than replaced. Technician B says...
asked 1 hour ago