Question

Comment on relative “activating strength” of methoxy and hydroxy groups in electrophilic aromatic substitution in bromination...

Comment on relative “activating strength” of methoxy and hydroxy groups in electrophilic aromatic substitution in bromination of vanillin (product being 5-bromovanillin)

Homework Answers

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Based on your result comment on the relative “activating strength” of methoxy and hydroxy groups in...
Based on your result comment on the relative “activating strength” of methoxy and hydroxy groups in electrophilic aromatic substitution. (product being 5-Bromovanillin) from reactin standard Vanillin with Acetic acid, Hydrobromic acid, and Potassium Bromate in a directive effect reaction
Organic II lab: Relative rates of electrophilic aromatic substituton reactions During the measurement of the relative...
Organic II lab: Relative rates of electrophilic aromatic substituton reactions During the measurement of the relative rate of electrophilic substitution on different aromatic compounds, how do you determine the reaction end-point? Explain your answer. _______________________________________________
1.Which of the following would react faster than benzene in an electrophilic aromatic substitution reaction? a....
1.Which of the following would react faster than benzene in an electrophilic aromatic substitution reaction? a. acetophenone b. benzoic acid c. anisole d. chlorobenzene 2.Which of the following would react slower than benzene in an electrophilic aromatic substitution reaction? a. benzaldehyde b. phenol c. toluene d. aniline 3.If an electrophile was added to acetophenone via an electrophilic aromatic substitution, at what position(s) of the ring would the electrophile add? a. ortho b. meta c. ortho d. para only 4.If an...
Electrophilic Aromatic Substitution//Nitration of Bromobenzene Reagents used: nitric acid, sulfuric acid, bromobenzene 1) During the isolation...
Electrophilic Aromatic Substitution//Nitration of Bromobenzene Reagents used: nitric acid, sulfuric acid, bromobenzene 1) During the isolation procedure of this lab, you are instructed to wash your crystallized product (crystallized from ethanol) withice-cold ethanol. Why is it important to use ice-cold ethanol as opposed toroom temperature ethanol?
The reaction to form 4-nitroacetanilide from the acetanilide by electrophilic aromatic substitution. Nitrating mixture is a...
The reaction to form 4-nitroacetanilide from the acetanilide by electrophilic aromatic substitution. Nitrating mixture is a mixture of concentrated sulfuric acid and concentrated nitric acid. Glacial acetic acid and acetanilide are used. i) For this experiment, a low temperature (< 30 °C) was maintained throughout the addition of the nitrating mixture. What was the main purpose for maintaining a low temperature? ii)How did you (or how could you) confirm that your product was 4-Nitroacetanilide and not some other compound? If...
This is an organic chemistry lab question.The experiment is on relative reactivities of some aromatic compounds....
This is an organic chemistry lab question.The experiment is on relative reactivities of some aromatic compounds. I'll give an overview of how what I did in the experiment and what i need help with. This might look like a lot but i really do need some help. I used 0.070ml of Anisole + 0.5ml of Glacial acetic acid. I added 1.00ml of bromine/hydrobromic acid. the mixture was heated for about 15 minuted (a moistened sodium disulfide wool apparatus was attached...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT