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Outline a detailed mechanism for the acid catalyzed hydration of 2-methyl-2-butene and name the major product according to the IUPAC names
Suppose a pharmaceutical company is developing a new antiviral drug for use in the treatment of aids. A 1% solution of the drug has a freezing point of 0.053C.
A) you are asked to prepare 100ml of an isotonic solution containing 1% of the drug in water for injection. Show your calculations.
B) Estimate E value for this antiviral drug if Liso is 4.8.
Why do phenols sometimes react differently from alcohols despite the presence of the same functional group?

Place the letters underneath the molecules from LEAST basic to MOST basic:

 

NH-   OH-   Br-   CH3CH2O-    F-    CH3CH3

Alkynes E and F have the molecular formula C8H14. Treating with either compound E or
F with excess hydrogen in the presence of a metal catalyst leads to the formation of octane.
Similar treatment of a compound G (C8H12) leads to a product with formula C8H16 while
compound E with O3/H2O and hot KMNO4/H2O yields a single product (H) has molecular
formula C8H14O4. What are the structures of E, F, G, and H. Write the appropriate IUPAC
Name of compound H.
three (3) ways of protein analysis.
Draw the mechanism for the reaction of 1-butyne with sodium amide followed by butanal following acidification. Use line angle structures
Approximately 12 billion kilograms of phosphoric acid (H3PO4) are produced annually for fertilizers, detergents, and agents for water treatment. Phosphoric acid can be prepared by heating the mineral fluoroapatite (Ca5(PO4)3F) with sulphuric acid in the presence of water.
Ca5(PO4)3F + 5H2SO4 + 10H2O 3H3PO4 + 5CaSO4.2H2O + HF
If every kilogram of fluoroapatite yields 396 g of phosphoric acid, what is the percent yield?
Calculate the concentrations of the major ionic species present in the 1.29 mL solution of 3.22 mg of Ba(HCO3)2.

An organometallic cyclic compound (E; C6H11MgBr) was synthesized by one of my PhDscholars followed by magnesium in dry ether which was further react with butanal to yielda macromolecule alcoholic compound (F) after mild acidification. Prolonged treatment of
F with an equivalent amount of hydrogen bromide to 1-bromo-1-butylcycloheptane (G).
Write the structures of (E) and (F), and explain how (G) is obtained from (F).

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