Williamson Ether Synthesis with a benzyl bromide derivative
Nucleophilic substitution involving sodium phenoxide
Williamson Ether Synthesis with alkoxide and alkyl sulfonate
Dehydration of alcohol using sulfuric acid at high temperature
Step 1: Understanding ether synthesis methods. Ethers (\({R-O-R'}\)) can be synthesized by several methods, but the Williamson Ether Synthesis is the most reliable and widely used approach.
Step 2: Identifying the correct reaction. - The Williamson Ether Synthesis involves the reaction of a sodium alkoxide (\({R-O}^-\)) with a primary alkyl halide or alkyl sulfonate (\({R'-X}\)).
- The given reaction in option C follows this method, where a sodium alkoxide reacts with an alkyl sulfonate to form an ether under mild heating.
Step 3: Eliminating incorrect Option.
- Option A: Involves a benzyl bromide derivative, which may lead to side reactions.
- Option B: Though nucleophilic substitution can form ethers, it is not as general or effective as the Williamson method.
- Option D: The acid-catalyzed dehydration of alcohol at high temperature (443 K, using \({H}_2{SO}_4\)) is used to form ethers, but this method is not ideal for unsymmetrical ethers and works mainly for primary alcohols.
Thus, the correct answer is (C) Williamson Ether Synthesis with alkoxide and alkyl sulfonate.
Which of the following represents double stranded helix structure of DNA?
At STP \(x\) g of a metal hydrogen carbonate (MHCO$_3$) (molar mass \(84 \, {g/mol}\)) on heating gives CO$_2$, which can completely react with \(0.02 \, {moles}\) of MOH (molar mass \(40 \, {g/mol}\)) to give MHCO$_3$. The value of \(x\) is:
Evaluate the following limit: $ \lim_{n \to \infty} \prod_{r=3}^n \frac{r^3 - 8}{r^3 + 8} $.
In the given cycle ABCDA, the heat required for an ideal monoatomic gas will be:
A particle is moving in a straight line. The variation of position $ x $ as a function of time $ t $ is given as:
$ x = t^3 - 6t^2 + 20t + 15 $.
The velocity of the body when its acceleration becomes zero is: