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- Identify the electrophile and the nucleophile in each of the following reaction steps. Then draw curved arrows to illustrate the bond-making and bond-breaking processes.Electrophilic aromatic substitution reactions require activating the nucleophile. True or FalseClassify the following species as an electrophile, necleophile or radical
- which combinations will favour a substitution reaction over an elimination reaction?QUESTION 7 Which of following statement is incorrect regarding aromatic electrophilic substitution reaction? EAS reaction goes through a carbocation intermediate The rate determining step is loss of proton to form the product Benzene acts as a nucleophile in the EAS reaction Bromine acts as a electrophile in the EAS reactionProvide a complete step-by-step mechanism for the following reaction. ОН Conc. H2SO4 heat
- To preview the image click here Indicate which compound will have highest and lowest Bronsted acidity. 1. Choose the correct option for Highest Bronsted acidity [Select] 2. Choose the correct option for Lowest Bronsted acidity [Select] A B `ОН H3C :0: :0: تصور DWhich of the following hydrolysis reaction is incorrecta) Draw all resonance forms of 3-hydroxybenzaldehyde and of the corresponding conjugate base. W hich conclusions can you draw for its acidity (pKa) in comparison to phenol?| b) Draw all resonance forms of 3-hydroxybenzaldehyde and of the corresponding conjugate base. Which conclusions can you draw for its acidity (pKa) in comparison to phenol and 3-hydroxybenzaldehyde? c) Discuss the relative acidities of 2-hydroxybenzaldehyd und 4-hydroxybenzaldehyd.