4. As we know that anthracene is a nonpolar aromatic hydrocarbon, so it will be inert in acids and bases which requires a polar medium.
Now, in case of 4-chloroaniline, which is obviously basic in nature due to its amine group, will react with dilute acids to give soluble salts.
Now, if we are given a mixture of the above two, there are practically TWO kinds of the separation method. One is simply on the basis of solubility in a polar medium. The other is using the basic character of the latter i.e just take the mixture and add any dilute acid (say, dilute HCl), and one will observe that the 4-chloroaniline getting dissolved by the formation of a chloride salt and the anthracene remaining insoluble withing the mixture. Then filter out the soluble part( which contain 4-chloroaniline) and add some dilute NaOH and the excess acid is neutralized and 4-chloroaniline is separated out from the mixture finally.
Н ОН -H HO HOS HOHT OH glucose Water will be soluble with glucose due available...
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...