Complete the following information for sodium.
Normal level
Functions
Major location
Mechanism(s) of electrolyte hemeostasis
Complete the following information for sodium. Normal level Functions Major location Mechanism(s) of electrolyte hemeostasis
Complete the following information for calcium. Normal level Functions Major location Mechanism(s) of electrolyte hemeostasis
Provide mechanism and Complete the following reactions by giving the major organic product(s), including stereochemistry. H3C CH3 Ph=C=C-Ph+ CEC (C20H22) light H3C CH3
Complete the electron pushing mechanism for the formation of the major product in the following reaction by adding any missing charges, atoms, bonds, non-bonding electrons, and curved arrows. Predict all the products of the reaction. Complete the electron pushing mechanism for the formation of the major product in the following reaction by adding any missing charges, atoms, bonds, non-bonding electrons, and curved arrows. Predict all the products of the reaction.
Write the product and a complete arrow-pushing mechanism and propose (the) major product(s) for the following transformation. After a Grignard reaction. .... Each of the Grignard reactions we have studied so far produces an alcohol as the major organic product. Alcohols can be used as starting materials for a number of organic reactions. Use this exercise to consider the range of reactions that can be performed after a Grignard reaction. For each reaction sequence below, suggest a Grignard reagent and...
Predict the major organic product of the following reaction and complete its mechanism below.
7. Draw the complete mechanism for the following reaction leading to the major product. ONa
Draw the major product and write the complete mechanism for the following reaction. Show resonance structures that lead to the formation of the major product.
s. Write out the complete mechanism, using curved arrows and all intermediate(s), of a first-order elimination of 3-chloro-3-methylpentane with sodium ethoxide in ethanol (8 points). Be sure to write out major and minor products, and indicate why each is major/minor (5 points). Indicate the name of each step, and identify which reagent is concentration-dependent, kinetically (2 points). 4. For the second-order substitution reactions below, draw the expected product(s), if any (6 points). CI NaBr OCH3 NaN3 2
Br 3. Show complete mechanism and intermediates formed in the following Sel process. OH + H ő heat ОН minor major 4. Determine if Sylor Sw2 mechanism is likely to take place based on conditions and show products for the following reactions. 1. 1-bromohexane reacting with sodium cyanide in acetonitrile (CH3CN) 2. tert-butyl iodide reacting with sodium acetate (CH3CO,Na) in acetic acid (CH,CO,H) 3. (S)-2-iodobutane reacting with potassium acetylide (NaC,H) in tetrahydrofuran 4. 1-bromo-1-methyl-cyclohexane reacting with water at 95°C.
Complete the electron pushing mechanism for the formation of the major product in the following reaction by adding any missing charges, atoms, bonds, nonbonding electrons, and curved arrows. Predict all the products of the reaction.