`HOCH_(2)-CH_(3)-underset(CH_(3))underset(|)(CH)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(2)OH`

Write IUPAC name of the following compound (a) CH_(3)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(2)underset(CH_(2)-CH_(3))underset(|)(CH)-CH_(2)-CH_(2)-CH_(3) (b) CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH_(2)-overset(CH_(2)-CH_(3))overset(|)(CH)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(3) (c)

Write IUPAC name of the following compound (a) CH_(3)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(2)underset(CH_(2)-CH_(3))underset(|)(CH)-CH_(2)-CH_(2)-CH_(3) (b) CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH_(2)-overset(CH_(2)-CH_(3))overset(|)(CH)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(3) (c)

CH_(3)-underset(OH)underset(|)CH-CH_(2)-underset(CH_(3))underset(|)CH-CHO

Write the IUPAC name of CH_(3)-CH_(2)-underset(CH_(2)OH)underset(|)(CH)-CH_(2)-underset(CH_(2)CH_(3))underset(|)(CH)-CH_(3)

Structures and IUPAC names of some hydrocarbons are given below. Explain why the names given in the parentheses are incorrect. underset(["and not 3,4,7-Trimethyloctane"])underset(2,5,6- "Trimethyloctane")(CH_(3)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(2)-underset(CH_(3))underset(|)(CH)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(3)) underset(["and not 5-Ethyl-3-methylheptane"])underset("3-Ethyl-5-methylheptane")(CH_(3)-CH_(2)-underset(CH_(2)CH_(3))underset(|)(CH)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(3))

Structures and IUPAC names of some hydrocarbons are given below. Explain why the names given in the parentheses are incorrect. underset(["and not 3,4,7-Trimethyloctane"])underset(2,5,6- "Trimethyloctane")(CH_(3)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(2)-underset(CH_(3))underset(|)(CH)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(3)) underset(["and not 5-Ethyl-3-methylheptane"])underset("3-Ethyl-5-methylheptane")(CH_(3)-CH_(2)-underset(CH_(2)CH_(3))underset(|)(CH)-CH_(2)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(3))

Identify number of chiral carbons in the following compounds (I) H_(3)C-underset(OH)underset(|)(CH)-underset(OH)underset(|)(CH)-underset(OH)underset(|)(CH_(2)) (II) H_(3)-underset(CH_(3))underset(|)(CH)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(2)

The decreasing order of rate of ester formation of the following compounds with acetic acid in presence of H^(+) ion is 1. CH_(3)-CH_(2)-CH_(2)-CH_(2)-OH 2. CH_(3)-CH_(2)-underset(OH)underset(|)(CH)-CH_(3) 3. CH_(3)-underset(CH_(3))underset(|)(CH)-CH_(2)-OH 4. CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-OH

CH_(3)-CH_(2)-underset(OH)underset(|)(CH)-underset(CH_(3))underset(|)(CH)-CHO

CH_(3)underset(NH_(2))underset(|)(CH)-CH_(2)CH_(2)underset(OH)underset(|)CHCH _(2)CH_(3)