Molecule: Atenolol
Question:
1. Indicate the 1-2 most electrophile site(s) in the
molecule.
2. Indicate the 1-2 most nucleophile site(s) in the molecule.
Molecule: Atenolol Question: 1. Indicate the 1-2 most electrophile site(s) in the molecule. 2. Indicate the...
Molecule: Atenolol Question: List hydrolyzable functional groups as well as various products that may be formed by treating the substance with diluted aqueous acid. olar HN OH
(14 pts) 2. Define electrophile. Give an example of charged molecule that reacts as an electrophile: Give an example of an electrophile that has a partial charge: Give an example of an electrophile that has no charge: Define nucleophile Give an example of a nucleophile that is charged: Give an example of a nucleophile that has a partial charge: Give an example of a nucleophile that has no charge:
0 to 3 correct answers corresponds to a FAIL (F). 4 or 5 correct answers is a PASS (P). Question 1: Circle all that apply for the site that has been circled. Nucleophilic Acidic Electrophilic Basic Question 2: Circle all that apply for the site that has been circled. OH Nucleophilic Acidic Electrophilic Basic Question 3: In the reagents of the following reaction indicate which molecule is the nucleophile and which molecule is the electrophile Р . +нсі OH +...
Select the most nucleophilic site on the molecule. 1) 2) 3) OH 5) NH2 4)
1) Label the acidic functional groups 2) For each acidic site, indicate if it has been drawn in the protonated form or not 9/1/16 Name: Worksheet 2 Below is a partial structure of Humic Acid, Circle AND name SEVEN different functional groups on the molecule НООС HOOC сно нс-он COOH --0 он НО. но-сн НО он ( ОН нс-он COOH о HC-OH с=0 o- НО но оноо ОН HN NH
Choose the most appropriate reagent(s) for the conversion of the amide to the amine target molecule. SOCI2 Ph OH Ph CI HN Ph N reagent(s) I- I- A H2, Pd B NaBH4, CH3OH © NaNH2, NHz 1. LiAIH4 2. H*, H20 E NH2NH2, KOH
3. Write the mechanism for an S 2 reaction using 1-butanol as your electrophile and HBr as your nucleophile.
No molecule x present 44 4 - Site 1 Site 1 Site 2 Site 2 — Low concentrations of molecule x Site 1 Site 2 High concentrations of molecule x 14444 Site 1 Site 2 When no molecule X is present, can the transcription factor A bind to either site on the DNA? Select] When there are low levels of molecule X, transcription factor A-X is able to bind to site 1. What can you tell about the affinity of...
2. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, product intermediate structure and name (please show which carbon carriers charges if possible)," chemistry is involved, please indicate "anti" or "syn" at the end of the reaction equation. Please name the product. Please indicate "follow Markovnikov's rule or not follow Markovnikov's rule". (If hydride shift is possible, please consider it and show it in your reaction) 1-1) Reaction of the following with HBr in electrophilic addition reactions H3PO4 2) pent-1-ene...
1. Write a chemical equation for 2-bromobutane with silver nitrate in ethanol. Identify the electrophile, nucleophile, precipitate and solvent. 2-bromobutane + CH3CH2OH + AgNO3 → 2. Write a chemical equation for 1-bromobutane with sodium iodide in acetone. Identify the electrophile, nucleophile, precipitate and solvent. 1-bromoburtane + CH3CH2OH + AgNO3 →