Why must the sodium hypochlorite in the electrophilic aromatic substitution reaction be added to the reaction mixture in ice?
Sodium hypochlorite (NaOCl) is highly unstable compound and decomposes explosively on heating. The compound decomposes rapidly at room temperature, so it must be kept under refrigeration. At lower temperatures, however, it is quite stable.
Decomposition occurs in sodium hypochlorite solutions at high or room temperature, forming sodium chlorate and sodium chloride.
3 NaOCl (aq) → 2 NaCl (aq) + NaClO3 (aq)
This decomposition reaction can also competes with chlorate formation, yielding sodium chloride and oxygen gas at room or high temperature.
2 NaOCl (aq) → 2 NaCl (aq) + O2 (g)
So, in simple words we can say that to prevent decomposition of Sodium hypochlorite, it is added to the reaction mixture in ice.
Why must the sodium hypochlorite in the electrophilic aromatic substitution reaction be added to the reaction...
7. Explain with the use of appropriate resonance structures, the regioselectivity of the electrophilic aromatic substitution reaction - i.e. why is electrophilic aromatic substitution of acetanilide less favoured at the 3-position than at the 2- or the 4-positions.
Nitration of phenols is a classic example of an electrophilic aromatic substitution reaction. a) Why does the nitration of phenol (hydroxybenzene) proceed only in the ortho- and para-positions on the ring? b) Draw the resonance structures that highlight the ortho- and para-directing nature of hydroxy substituents. Make sure to include the structures that showcase the movement of the charges in the ring.
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:...
Mechanism.Provide a mechanismto account for formation of the
product of thefollowing Electrophilic Aromatic Substitution
reaction.
Mechanism. Provide a mechanism to account for formation of the product of the following Electrophilic Aromatic Substitution reaction. D. OX Reactions. Please complete the following reaction schemes. Molaro NH2 FeCl3 H300 OCH3 H2CO OCH3
Write the mechanism for an electrophilic aromatic substitution reaction given any aromatic compound and either chlorine, Cl2, or t-butyl cation as the electrophile
Reactions of aromatic compounds are: -Addition -Reduction -Electrophilic aromatic substitution -Nucleophilic aromatic substitution
where would the electrophile end up if the following molecule
underwent an electrophilic aromatic substitution reaction.
QUESTION 9a: Where would the electrophile end up if the following molecule underwent an electrophilic aromatic substitution reaction? Briefly explain your reasoning
In the following compound, select the position that is most
reactive towards electrophilic aromatic substitution
reaction.
Review of Skills - Skill Builder 18.03 X Incorrect. Tert-butyl (activator) will direct the incoming electrophile and it is an ortho-para director. In the following compound, select the position that is most reactive towards electrophilic aromatic substitution reaction. NO,
!!! If each compound undergoes electrophilic aromatic substitution, where should the substituent be added? *The choices for each are either ortho/para position OR meta position.* Phenol? Benzaldehyde? Benzoic Acid? Bromobenzene? Nitrobenzene? Toluene?
Nitration of an aromatic ring involves an electrophilic
substitution reaction. Draw the structure of the electrophile that
is attacked by the aromatic ring and the intermediate formed after
attachment of the electrophile to the ring. Be sure to show formal
charges.