(S)-3-Chloro-1-pentene reacts with sodium ethoxide in ethanol to produce 3-ethoxy-1-pentene. The reaction is second order, being first order in 3-chloro-1-pentene and first order in sodium ethoxide. (a) Complete the following statements about this reaction. The reaction proceeds via an The stereochemistry of the product is In the absence of sodium ethoxide, 3-chloro-1-pentene reacts with ethanol to produce both 1-ethoxy-2-pentene and 3-ethoxy-1-pentene. (b) Complete the following statements about this reaction. The reaction proceeds via an The stereochemistry of 1-ethoxy-2-pentene is The stereochemistry of 3-ethoxy-1-pentene is Draw the structure of the intermediate's resonance contributor that leads to the formation of 3-ethoxy-1-pentene. W + go 85 mechanism. **11 mechanism. ? ?
(S)-3-Chloro-1-pentene reacts with sodium ethoxide in ethanol to produce 3-ethoxy-1-pentene. The reaction is second order, being first order in 3-chloro-1-pentene and first order in sodium ethoxide. (a) Complete the following statements about this reaction. The reaction proceeds via an The stereochemistry of the product is In the absence of sodium ethoxide, 3-chloro-1-pentene reacts with ethanol to produce both 1-ethoxy-2-pentene and 3-ethoxy-1-pentene. (b) Complete the following statements about this reaction. The reaction proceeds via an The stereochemistry of 1-ethoxy-2-pentene is The stereochemistry of 3-ethoxy-1-pentene is Draw the structure of the intermediate's resonance contributor that leads to the formation of 3-ethoxy-1-pentene. W + go 85 mechanism. **11 mechanism. ? ?
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Transcribed Image Text:(S)-3-Chloro-1-pentene reacts with sodium ethoxide in ethanol to produce 3-ethoxy-1-pentene. The reaction is second order, being first order in 3-chloro-1-pentene and first
order in sodium ethoxide.
(a) Complete the following statements about this reaction.
The reaction proceeds via an
The stereochemistry of the product is
In the absence of sodium ethoxide, 3-chloro-1-pentene reacts with ethanol to produce both 1-ethoxy-2-pentene and 3-ethoxy-1-pentene.
(b)
Complete the following statements about this reaction.
The reaction proceeds via an
The stereochemistry of 1-ethoxy-2-pentene is
The stereochemistry of 3-ethoxy-1-pentene is
Draw the structure of the intermediate's resonance contributor that leads to the formation of 3-ethoxy-1-pentene.
W
+
go 85
mechanism.
**11
mechanism.
?
?
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