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19 Nov 2019
8:24 PM OO Sprint F ttu black board.com 1. Where would the M+ peak be on a mass spec spectrum be for the following compound? B. 142 C. 147 53 2. What functional groups are present in the molecule shown to the right? AL Aromatic Ring, Ketone, Alkyne, Ether, Amine B. Aromatic Ring. Carboxylic Acid, Alkene. Ether, Amine C. Aromatic Ring. Carboxylic Acid. Alkene, Ester, Amide D. Aromatic Ring, Ketone, Alkyne, Ester, Amide E. Aromatic Ring, Ketone, Carboxylic Acid, Ether, Amine, Ester 3. In this reaction, does NO act like a Lewis acid, Lewis base, Bronsted acid or Bronsted base? A. Lewis Acid B. Lewis Base C. Bronsted D. Bronsted Base E. Lewis Acid and Bronsted Acid 4. Given the following reactions determine whether each will favor the products or the reactants: Reaction 1: Acetylide Ethanol Acetyl Ethoxide (pKa Acetylene 25. pKa ene Ethanol 16) Reaction 2: Ethoxide lon Hydrocyanic Acid Ethanol Cyanide lon (pKa Ethanol-16, pKa Hydrocyanic Acid-9.3) A. Reaction favors products. Reaction 2 favors products B. Reaction I favors products. Reaction 2 favors reactants C. Reaction I favors reactants, Reaction 2 favors products D. Reaction 1 favors reactants, Reaction 2 favors reactants 5. Which of the following is not a valid resonance structure of the other 4 30%
8:24 PM OO Sprint F ttu black board.com 1. Where would the M+ peak be on a mass spec spectrum be for the following compound? B. 142 C. 147 53 2. What functional groups are present in the molecule shown to the right? AL Aromatic Ring, Ketone, Alkyne, Ether, Amine B. Aromatic Ring. Carboxylic Acid, Alkene. Ether, Amine C. Aromatic Ring. Carboxylic Acid. Alkene, Ester, Amide D. Aromatic Ring, Ketone, Alkyne, Ester, Amide E. Aromatic Ring, Ketone, Carboxylic Acid, Ether, Amine, Ester 3. In this reaction, does NO act like a Lewis acid, Lewis base, Bronsted acid or Bronsted base? A. Lewis Acid B. Lewis Base C. Bronsted D. Bronsted Base E. Lewis Acid and Bronsted Acid 4. Given the following reactions determine whether each will favor the products or the reactants: Reaction 1: Acetylide Ethanol Acetyl Ethoxide (pKa Acetylene 25. pKa ene Ethanol 16) Reaction 2: Ethoxide lon Hydrocyanic Acid Ethanol Cyanide lon (pKa Ethanol-16, pKa Hydrocyanic Acid-9.3) A. Reaction favors products. Reaction 2 favors products B. Reaction I favors products. Reaction 2 favors reactants C. Reaction I favors reactants, Reaction 2 favors products D. Reaction 1 favors reactants, Reaction 2 favors reactants 5. Which of the following is not a valid resonance structure of the other 4 30%
Nelly StrackeLv2
23 May 2019