ANS:
A) Nitration of Methyl Benzene gives Ortho Methyl Benzene formation is Favourable( 63%).
B) Nitration of Benzoic acid gives meta- Nitrobenzoic acid formation is favorable ( 80%).
C) Nitration of Bromo Benzene gives Para- Nitro bromo benzene .
The details find from images below attached.
perform a nitration RXN on A.) Nylu un methyl group, CH3 WW - COOH od Br...
QUESTION 10 You perform a nitration reaction on this reactant It is a carboxylic acid COOH how fast do you think the reaction will occur relative to 7 Where do you think the new nitro group will be placed? Rate will be decreased. Nitro will be meta Rate will be decreased Nitro will be ortho or para Rate will be increased. Nitro will be meta Rate will be increased. Nitro will be ortho or para
Nitration of 1,3-dimethylbenzene primarily occurs at: Carbon 5 because the nitro group is meta directing carbon 2 because methyl groups are ortho/para directing Carbon 4 or 6 because the methyl groups are ortho/para directing Carbon 5 because the methyl groups are meta directing The conversion of an alcohol into an alkyl chloride by reaction with thionyl chloride is best described as an example of: an SN2 process an SN1 process an E2 process an electrophilic addition process an E1 process...
1- The product of the nitration reaction will have a nitro group at which position with respect to the methyl group? mostly para mostly ortho ortho and para at a 50:50 ratio meta 2- According to Sigma, what is the theoretical melting point of the para nitration product? 54 °C 243 °C It decomposes at 300 °C 155 °C 3- What is the MAIN safety concern with respect to how you handle waste for this lab? Using acid/base indicators. Don't...
Add the following questions to the final report: a) Why does the carbomethoxy group directs the reaction to positions that are meta to it? b) Why the formation of dinitrobenzaote is substantially disfavored ? c) Would you expect small amounts of the ortho and para substituted product? How would you remove them if they are formed ? d) Why does water have a retarding effect on the nitration ? e) Explain why Benzene has lower reactivity in electrophilic addition reactions...
Hello everyone, I'm having serious doubts about my answers for this activity and I need help. Instructions for this activity: How would you synthesize the following substances starting from benzene? Assume that ortho- and para- substitution products can be separated. Show all reactions. My answers: 1 - 3 4 - 6 7 - 9 10 Your help will be much appreciated! 1. C-huelcony melly I heezerve OH 044 Freidel Crafts pikylation. CH₃ G Oxidation N20 + CH₂Cl AlCl₃ Benzene Phenol...
the weight if the initial product was 3.4 grams of methyl benzoate. Who |o yald foR 3.91SSg st prodoct nd product 2.14143 EXPERIMENTAL PROCEDURE SAFETY WEAR nitrile gloves for this experiment. The nitrating moture of sulfuric acidnitric acid (1:1) is a very strong acid system. Do not allow it to come in contact with your skin or clothing. It will cause acid burns if it comes in contact with your skin (and holes an your clothes). Wash any affected area...
Read the articles provided (Riggio, 2008) and Javidan & Walker (2012). Perform a self-assessment of the global mindset competencies. What competencies do you feel are your strengths? Your areas for improvement? What next learning steps could you take to address your areas for improvement? LEADERSHIP DEVELOPMENT: THE CURRENT STATE AND FUTURE EXPECTATIONS Ronald E. Riggio Claremont McKenna College This article discusses the common themes in this special issue of Consulting Psychology Journal on "Leadership Development" and summarizes some of the...