1. Write the reaction that you will do this week for the Williamson ether synthesis. Label the nucleophile and the electrophile, the nucleophilic atom and the electrophilic atom. 2. Mechanistically, what type of reaction is the ether synthesis that you will perform this week? 3. An extraction is done for the work-up. What liquids will be used for the extraction? In which liquid will the product be? Will the product be in the top layer or the bottom layer?
Reactive Intermediates
In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.
Hydride Shift
A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.
Vinylic Carbocation
A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.
Cycloheptatrienyl Cation
It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.
Stability of Vinyl Carbocation
Carbocations are positively charged carbon atoms. It is also known as a carbonium ion.
1. Write the reaction that you will do this week for the
2. Mechanistically, what type of reaction is the ether synthesis that you will perform this week?
3. An extraction is done for the work-up. What liquids will be used for the extraction? In which liquid will the product be? Will the product be in the top layer or the bottom layer?
![**Transcription for Educational Website:**
This diagram illustrates the Williamson Ether Synthesis, a reaction that produces an ether from an alkoxide and a haloalkane.
**Reactants:**
- **Sodium ethoxide (\(C_2H_5ONa\))**: A base that contributes the ethoxide ion.
- **1-Bromobutane (\(C_4H_9Br\))**: A reactant with a boiling point of 101°C and a density of 1.27 g/mL.
**Reaction Conditions:**
- The reaction takes place in ethanol as the solvent at a temperature of 90°C.
**Products:**
- **1-Ethoxybutane (\(C_6H_{14}O\))**: The target ether product, with a boiling point of 91-92°C and a density of 0.75 g/mL.
- **Sodium bromide (NaBr)**: A byproduct of the reaction.
**Reaction Pathway:**
- The ethoxide ion from sodium ethoxide attacks the electrophilic carbon in 1-bromobutane, resulting in the formation of 1-ethoxybutane and the release of sodium bromide.
This reaction is an example of nucleophilic substitution and demonstrates the classic method for synthesizing ethers.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F39f6380b-55e3-47ff-8091-2f92e2b304db%2F34e02d1d-5005-47e7-b20d-bc4fb32460b1%2F5cxqd1_processed.png&w=3840&q=75)
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