What best describes carbocations? Lewis acids and electrophilic Lewis bases and electrophilic Lewis acids and nucleophilic Lewis bases and nucleophilic
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- 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.Rank the following carboxylic acids from least to most acidic.help with carboxylic acid reactions
- Show reaekson and don't use hend raiting and step by step solutions pleaseWhich 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 acidFor each molecule below, draw the conjugate acid or conjugate base or both if the molecule hasboth a conjugate acid and a conjugate base (e.g., water).
- For the following acid-base reaction, predict which side of the equilibrium is favored. H u.of-u.a CH -N-H N favor left side favor right side neither HShaw haw structure A. बगाण दण u are able to get strcture B from gok you Hint There are 5 Steps Ht transfer Neucleo philic addition H20 is tne nueleophile to be added profan transfer Proton fransfer proton transterSelect the stronger base and then draw its conjugate acid below. CICH₂CH₂O or CH3CH₂O- • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • You do not have to include lone pairs in your answer. Ⓡ OO. n[1] ? ChemDoodle