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Principal functional group-Polyfunctional Organic Compounds
If the organic compound includes two or more functional groups, one of the functional sets is chosen as the principal functional group whereas all the remaining functional groups (as well called the secondary functional groups) are treated as substituents. The subsequent order of preference is used when selecting the principal functional group.
Sulphonic acids > carboxylic acids > anhydrides > esters > acid chlorides > acid amides > nitriles > aldehydes > ketones > thiols > alcohols >alkenes > alkynes.
All the remaining functional sets like halo (fluoro, chloro, bromo, iodo), nitroso (-NO), -nitro (-NO2), amino (-NH2) and alkoxy (-OR) are treated like a substituents.
Acidic Nature of Phenol - Hydrocarbon The acidic nature of phenol is observed in the following: (1) Phenol changes blue litmus to red. (2) Highly electropositive metals r
Q. How many centigrams are in 5 kilograms? Two conversion factors are essential to solve this problem. Keep in mind that there are 1000 grams in a kilogram and 100 centigrams i
Short note of synthesis of dry and bhc
Which of the following conduct electricity in the fused state: (1) BeCl 2 (2) MgCl 2 (3) SrCl 2
Q. Explain Valence Bond Theory? This concept starts with the assumption that the bond between the metal ion and the ligand is basically covalent in nature. In order to form a c
Pyroligneous acid - Aldehydes and Ketones Pyroligneous acid consisting of acetic acid, acetone and methyl alcohol that is distilled in copper vessel and the vapours are passed
explain the bonding and structure in transition metal carbonyls
4-nitrotolouene ---> LiAlH 4 converts it to 4-aminotoluene ----> Add HNO 2 and it forms -----> diazonium salt ------> add H 3 PO 2 to get Toluene -----> add Br 2 /CCl 4 - 2
how condensation being done??
This is an acid-catalyzed addition to the double bond much like hydration, except that an alcohol rather than water is the nucleophile that reacts with the carbocation intermediate
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