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- In SN2 reactions of haloalkanes, the order of reactivity is RI>RBr>RCl>RF. Alkyl iodides are considerably more reactive than alkyl fluorides, often by factors as great as 106. All 1-halo-2,4-dinitrobenzenes, however, react at approximately the same rate in nucleophilic aromatic substitutions. Account for this difference in relative reactivities.Dr@w a carbene and explain how it can function as a nucleophile or electrophile.17. Which aromatic compound in figure 17 will be least reactive in an electrophyllic aromatic substitution reaction?
- Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict the major products of the reactions of naphthalene with isobutylene and HFElectrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict the major products of the reactions of naphthalene with HNO3, H2SO4.Which of the following is the major organic product in the reaction sequence in Image 21? A. b B. c C. a D. d
- Compound name is Toluene . Name the structures of all possible chemical (Electrophilic aromatic substitution) reactions of the compound namely; a. Halogenation (Chlorination or Bromination) b. Nitration c. Sulphonation d. Friedal Craft Alkylation e. Friedai need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?
- H8. Organic chemistry Text answers and (descriptive structures and / or reaction mechanisms). Explain the chemistry of the carbonyl group (direct addition of nucleophiles and addition with elimination)What are the steps of the mechanism of reaction . Electrophilic aromatic substitution. Is it Ortho,para,meta ?In electrophilic aromatic substitution reaction by drawing the structures of the compounds given below Explain which products will be formed as a result of the reaction with the nitronium ion.a)Methoxybenzeneb)Benzoic acid