In each reaction box, place the best reagent and conditions from the list below.
1 answer:
This is a two step step reaction as shown below,
Step 1:
Epoxidation of Alkene:
In first step Cyclohexene is treated with peroxybenzoic acid in the presence of Dichloromethane which results in the formation of epoxide moiety.
Step 2:
Nucleophillic Substitution Reaction:
In second step the epoxide formed is treated with Sodium Methoxide which acts as a nucleophile and attacks the less hindered carbon of epoxide resulting in the formation of final product as shown below.
Step 1:
Epoxidation of Alkene:
In first step Cyclohexene is treated with peroxybenzoic acid in the presence of Dichloromethane which results in the formation of epoxide moiety.
Step 2:
Nucleophillic Substitution Reaction:
In second step the epoxide formed is treated with Sodium Methoxide which acts as a nucleophile and attacks the less hindered carbon of epoxide resulting in the formation of final product as shown below.
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Answer:
sp³d¹ hybridization
Explanation:
Given Cl as central element with three F substrates ...
The VSEPR structure indicates 5 hybrid orbitals that contain 2 diamagnetic orbitals (non-bonded e⁻-pairs) and 3 paramagnetic orbitals (single, non-paired electron for covalent bonding with fluorine) giving a trigonal bypyrimidal parent with a T-shaped geometry.
Valence bond theory predicts the following during bonding:
Cl:[Ne]3s²3p²p²p¹3d⁰
=> [Ne]3s²p²p¹p¹d¹
=> [Ne]3(sp³d)²(sp³d)²(sp³d)¹(sp³d)¹(sp³d)¹
giving 3 ( [Cl](sp³d) - [F]2p¹ ) sigma bonds and 2 non-bonded pairs on Cl.
Note the following images:
Non-bonded electron pairs are in plane of parent geometry and Fluorides covalently bonded to central element Chloride forming the T-shaped geometry.
