All please Q5) Which one of the following is(are) required for the Halogenation of aromatics?A] CatalystB] FeClaCJ Surfuric AcidD] FeCl₂Q6) Which one of the following is(are) active electrophile(s) for Halogenation ofaromatics?A FeClsB FeCl₂A carbocationC FeCl3Q7) In Friedel-Crafts alkylation reaction, which one of the following is(are) activeelectrophile(s)?D Not listed hereB carboanion. C Aluminum trichloride D Not listed hereQ8) Which statement is true for Aluminum in AICI3?A] Oxophilic B] Nucleophilic C] Bronstead AcidD] OxyphilicQ9) Why Friedel-Crafts alkylation reaction is not recommended to employ in preparationof alkyl benzene with a primary connection?(A) It is a slow reaction(B) It generates primary carbocation which is very reactive toward benzene(C) Yield mixture of products(D) both (B) and (C)

Note: According to our guidelines we are supposed to answer only first three questions. Kindly…

Q5) Which one of the following is(are) required for the Halogenation of aromatics? A] Catalyst B] FeCla C] Surfuric Acid D] FeCl₂ Q6) Which one of the following is(are) active electrophile(s) for Halogenation of aromatics? A FeCls B FeCl₂ A carbocation Q7) In Friedel-Crafts alkylation reaction, which one of the following is(are) active electrophile(s)? B carboanion C FeCl3 10 D Not listed here C Aluminum trichloride D Not listed here

Q5) Which one of the following is(are) required for the Halogenation of aromatics? A] Catalyst B] FeCla C] Surfuric Acid D] FeCl₂ Q6) Which one of the following is(are) active electrophile(s) for Halogenation of aromatics? A FeCls B FeCl₂ A carbocation Q7) In Friedel-Crafts alkylation reaction, which one of the following is(are) active electrophile(s)? B carboanion C FeCl3 10 D Not listed here C Aluminum trichloride D Not listed here

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter6: Reactions Of Alkenes

Section: Chapter Questions

Problem 6.27P: Reaction of this bicycloalkene with bromine in carbon tetrachloride gives a trans dibromide. In both...

See similar textbooks

Similar questions

For each section, circle the mechanism from the two options given (SN1 or SN2) and draw the main organic product resulting from that mechanism. Indicate the stereochemistry and if two configurational isomers form, draw both.
Draw the major organic product of each reaction. Indicate the stereochemistry at the stereogenic center. Omit byproducts such as salts. If applicable, expand octets to minimize formal charges.
Which of the following species are conjugated?
Rank from decreasing reactive to most reactive (SN1)
Which of the following reactions will have the faster rate and give a better yield? Use drawings of the transition state (show orbitals!) to explain why.
Fill in the missing reactant along with optically active or racemic name and what reaction it goes by E1, E2, SN1, OR SN2
What are the possible constitutional isomers and rank by SN2 reaction.
What is the product E and how is it formed? Can this be explained using frontier molecular orbital analysis? What would the regiochemistry and stereochemistry be?
Not sure what substitution goes here for the SN2 reaction
Among the choices, what is (a) a conjugated diene, (b) a meso compound, (c) enantiomer of FOR and (d) diastereomer of SHE
a) Predict the major product of the reaction and identify the type of reaction (substitution or addition). Explain the function of Pt used in the reaction. (with First image) b) Write the reaction of the mononitration of chlorobenzene and predict the major products with reasons. c) Identify all the carbon atoms in the following compounds that are sp2 (Circle the carbon(s) your selected on image two)
Why does the diene need to be in the s-cis conformation to yield the cyclic product?