Given below are two statements: Statement (I): Neopentane forms only one monosubstituted derivative. Statement (II): Melting point of neopentane is higher than n-pentane In the light of the above statements, choose the most appropriate answer from the options given below:

Solution & Explanation

### Related Formula textSymmetric Structure propto textMelting Point (Packing efficiency) ### Core Logic **Statement (I) is correct**: Neopentane (2,2-dimethylpropane) contains a quaternary carbon bonded to four methyl groups. There are 12 hydrogen atoms, all of which are primary and chemically equivalent. Halogenation yields exactly one monosubstituted derivative: mathrm(CH_3)_4C + X_2 xrightarrowhnu (CH_3)_3C-CH_2X + HX Statement (II) is correct: Neopentane has a compact, symmetrical, nearly spherical molecular structure. In the solid crystal lattice, these spherical molecules pack much more efficiently compared to the floppy, linear n-pentane. This robust crystalline packing dramatically increases its melting point (256.4~mathrmK) compared to that of n-pentane (143.4~mathrmK). ### Step 1: Final Verification Since both statements are theoretically and experimentally correct, the correct option is (2).
Alkanes and Physical Properties
Alkanes and Physical Properties
### Pattern Recognition While branching *decreases* the boiling point (due to decreased surface area and weaker van der Waals forces), branching that creates a highly symmetric structure *increases* the melting point because of close-packing efficiency in the solid phase. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Hydrocarbons

More Hydrocarbons Previous-Year Questions — Page 5

Q84 jee_main_2024_31_jan_evening Halogenation of Alkanes (Isomers)
Number of isomeric products formed by mono-chlorination of 2-methylbutane in presence of sunlight is ________
Numerical Answer. Answer: 6 to 6

Solution

### Core Logic The structure of 2-methylbutane is CH_3-CH(CH_3)-CH_2-CH_3. It has four different types of hydrogen atoms, which can be substituted to form structural isomers: 1) 1-chloro-2-methylbutane: Chlorination at terminal CH_3 near branch. Yields a chiral center at C2 (2 enantiomers). 2) 2-chloro-2-methylbutane: Chlorination at the tertiary carbon (1 achiral product). 3) 2-chloro-3-methylbutane: Chlorination at the CH_2 group. Yields a chiral center at C2 (2 enantiomers). 4) 1-chloro-3-methylbutane: Chlorination at the far terminal CH_3. No chiral center (1 achiral product).
Halogenation of Alkanes (Isomers) diagram for Q84 - JEE Main 2024 Evening
Halogenation of Alkanes (Isomers) diagram for Q84 - JEE Main 2024 Evening
### Step 1: Counting Stereoisomers Total isomeric products = 2 (from 1st) + 1 (from 2nd) + 2 (from 3rd) + 1 (from 4th) = 6. ### Pattern Recognition When asked for "isomeric products" in halogenation without specifying "structural isomers", you must count stereoisomers (enantiomers) as well. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Hydrocarbons Class 12 Chemistry: Haloalkanes and Haloarenes
Q87 jee_main_2024_31_jan_morning Kolbe's Electrolysis
Number of alkanes obtained on electrolysis of a mixture of CH_3COONa and C_2H_5COONa is
Numerical Answer. Answer: 3 to 3

Solution

### Core Logic Kolbe's electrolytic method generates free radicals at the anode, which then combine to form alkanes. The given mixture yields two types of carboxylate radicals which decarboxylate to form alkyl radicals: CH_3COONa rightarrow dotCH_3 C_2H_5COONa rightarrow dotC_2H_5 These radicals can couple in three different ways: 1. Cross coupling: dotCH_3 + dotC_2H_5 rightarrow CH_3-CH_2-CH_3 (Propane) 2. Self-coupling 1: dotCH_3 + dotCH_3 rightarrow CH_3-CH_3 (Ethane) 3. Self-coupling 2: dotC_2H_5 + dotC_2H_5 rightarrow CH_3-CH_2-CH_2-CH_3 (Butane) Thus, a total of 3 different alkanes are formed. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Hydrocarbons
Rankbit System
JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%) | JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%)