What best describes carbocations? Lewis acids and electrophilic Lewis bases and electrophilic Lewis acids and nucleophilic Lewis bases and nucleophilic
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- Select all that belongs to "Electrophile" accepts an electron pair to form a bond donates an electron pair to form a bond Weak Lewis Acid Electron rich Electron poor Substitutes leaving group in Sn1 and Sn2 reactions Partially positive Strong Lewis Acid MacBook Air F6 F7 F8 F9 F10 F4 F5 % & 5 6 7 8Draw the products of each Lewis acid–base reaction. Label the electrophile and nucleophile.Which is the more stable base? a. Br− or I− b. CH3O− or CH3S− c. CH3CH2O− or CH3COO− d. H2C CH or HC C− e. FCH2CH2COO− or CH2CH2COO- f. CLCH2CH2O- or CL2CHCH2O-
- In each reaction, Label the reactants as a Lewis base (nucleophile) or a Lewis acid (electrophile). Use curved arrows to show the movement of electron pairs in the reaction. NH, H-C- H- H. ONH3Which N atom in chloroquine is the strongest base?The blcyclic ketone shown below is first treaterd with a base, then ethyliodide is added to form the substituted ketone. Which base/conditions are sultable? 1) Base 2) O 1. Lithium diisopropylamide in THF at -78 "C. O 2. NaBH4 in methanol at room temperature. O 3. Sodium methoxide in methanol at room temperature. O 4. DBU in THF at 25 "C.
- Please help me with these. The blank at the bottom could possibly be no reaction.Classify each reaction as either a proton transfer reaction, or a reaction of a nucleophile with an electrophile. Use curved arrows to show how the electron pairs move.Which of the following is the strongest acid? O a. acetic acid O b. dichlorobenzoic acid O c. dihydroxybenzoic acid Od. dichloro acetic acid e. chlorobenzoic acid