1.The best way to describe the "arrow" showing the mechanism of EAS is:
A.it goes from the attacking atom (electrophile) to the carbon being attacked.
B.it goes from the attacking atom to the new bond being formed.
C.it goes from the electron pair in the pi-bond on the ring to the new sigma bond being formed.
D.it involves a half-head arrow from the attacking species and a half-head arrow from the pibond to the new sigma bond to be formed.
2.In general, electrophilic aromatic substitution (EAS) happens:
A.between any aromatic molecule and an appropriate electrophile, assuming aromaticity follows the 2(n + 2) rule.
B.with any pi-bond containing molecule and an electrophile.
C.with chlorine or bromine and iron catalysis on any pi-bond species.
D.when an electrophile bonds to a nucleophile of some kind.
3.EAS with chlorine gas bubbled into chlorobenzene containing aluminum trichloride would:
A.not happen because chlorine is deactivating.
B.gives mostly meta-dichlorobenzene with mild heating.
C.gives mostly ortho-dichlorobenzene with mild heating.
D.generates HCl and mostly para-dichlorobenzene.
4. Fuming nitric acid converts phenol into:
A.pure trinitrophenol (also called "picric acid" which has a really low pKa for a phenolic compound).
B.2, 4-dinitrophenol because of deactivation with each nitro group added.
C.para-nitrophenol since the OH group on an aromatic ring is activating and ortho-para directing.
D.a complex mixture of ortho- and para-substituted phenols with di- and trinitro derivatives predominating.
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1.The best way to describe the "arrow" showing the mechanism of EAS is: A.it goes from...
6) The compound that can undergo self-condensation in the presence of NaOMe in MeOH Part 1: [20 marks] Select the best answer for each of the following: 1) Circle the species that is aromatic: [0][0] [] [O] 7) The most acidic compound Ola Tyra oko sya om ugungano 2) Circle the structure that has a heteroatom lone pair in the aromatic pi electron system 8) Each of the following disubstituted aromatics shown below is nitrated. In which of these cases...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...