What is the preferred position of nitration for each? (meta, para, ortho)

Question

Question

Answer 1

Answer #1

a) -No, attacts m-potih on Crneta) ecaux b) 130 No, Cmeba) otH3 oeH3 cl Pak

Answer 2

Similar Homework Help Questions

Classify each substituent as ortho, para activators; ortho, para deactivators; or meta deactivators. ortho, para activators...

Classify each substituent as ortho, para activators; ortho, para deactivators; or meta deactivators. ortho, para activators ortho, para deactivators meta deactivators CHO COon NH2 C(CH3)a
Could we have used IR to differentiate between the ortho, meta, and para isomers? Why or...

Could we have used IR to differentiate between the ortho, meta, and para isomers? Why or why not? Reaction 1: Nitration HNO3 NO2 + + H2SO4, H20 NO2 toluene NO2 ortho meta para
why is 16.17 in ortho and para position instead of meta position? Problem 16.17 d HNO3...

why is 16.17 in ortho and para position instead of meta position? Problem 16.17 d HNO3 Hasda O2N1 NO Problem 16.26 a SO,H Cl2 SOH so, H2SO4 FeCl3

Considering 1H-NMR analysis of substituted benzenes (for ortho, para, meta nitrobromobenzene and ortho, para dinitro bromobenzene,...

Considering 1H-NMR analysis of substituted benzenes (for ortho, para, meta nitrobromobenzene and ortho, para dinitro bromobenzene, or meta para dinitrobromobenzene) : What is the splitting patterns for ring hydrogens for the substituted benzenes? Using ??3-bond and 4-bond J coupling constants, what are: ??Relative chemical shifts of ring hydrogens?
In nitration of acetanilide(synthesis of p-nitroaniline) main product is ortho and para. Explain why ortho and...

In nitration of acetanilide(synthesis of p-nitroaniline) main product is ortho and para. Explain why ortho and para product is major in resonance and mechanism term.
An NH2 substituent in an aromatic ring is: Select one: a. activating ortho-, meta- and para-directing...

An NH2 substituent in an aromatic ring is: Select one: a. activating ortho-, meta- and para-directing b. deactivating and ortho- and para-directing c. deactivating and meta-directing d. activating and meta-directing e. activating and ortho- and para-directing

Table 1: AM1 Energies of the carbocations formed from nitration of the named compound (kcal/mol) ...

Table 1: AM1 Energies of the carbocations formed from nitration of the named compound (kcal/mol) ortho meta para Toluene (S = CH3) 221.74 224.49 219.04 Phenol (S = OH) 179.10 193.32 177.44 Trifluorotoluene (S = CF3) 95.17 90.06 93.56 Methyl benzoate (S = CO2CH3) 160.00 159.34 159.34 Using the table answer the following questions. 1 a. The carbocation intermediates are good models of the transition states for the corresponding aromatic reactions. When looking at the transition state energy of two...
i know that C is a meta director, but are any of these ortho or para,...

i know that C is a meta director, but are any of these ortho or para, or any other kind of directors? thanks! 4. Which of the following is a meta director?
Sort the following molecules by whether the substituent group is ortho/para or meta directing for electrophilic...

Sort the following molecules by whether the substituent group is ortho/para or meta directing for electrophilic aromatic substitution. Sort the following molecules by whether the substituent group is ortho/para or meta directing for electrophilic aromatic substitution.