The alkane which is next to methane in the homologous series can be prepared from which of the following reactions?
II, IV only
Step 1: Understanding the homologous series
The homologous series of alkanes consists of compounds differing by a -CH2- group. The alkane next to methane is ethane (C2H6).
Step 2: Evaluating the given reactions
1. Reaction I: Wurtz Reaction
2CH3Br + 2Na → dry ether C2H6 + 2NaBr
This reaction successfully forms ethane, making it a correct method.
2. Reaction II: Decarboxylation of Carboxylic Acids
CH3COOH + NaOH → CaO, Δ CH4 + Na2CO3
This reaction produces methane, not ethane, so it is incorrect.
3. Reaction III: Hydrogenation of Ethene
CH2CH2 + H2 → Pt C2H6
This reaction forms ethane, but it is not the best preparative method for homologous series alkane synthesis.
4. Reaction IV: Reduction of Alkyl Halides
CH3CH2Br + 2[H] → Zn/H+ C2H6 + HBr
This reaction also produces ethane, making it a valid method.
Step 3: Evaluating the Given Options
Thus, the correct answer is Option (1).
The reactions which cannot be applied to prepare an alkene by elimination, are
Choose the correct answer from the options given below:
An alkene X (\( C_4H_8 \)) on reaction with HBr gave Y (\( C_4H_9Br \)). Reaction of Y with benzene in the presence of anhydrous \( AlCl_3 \) gave Z which is resistant to oxidation with \( KMnO_4 + KOH \). What are X, Y, Z respectively?
Which of the following alkenes is most stable?