Draw the major organic product for the reaction of 1-phenylpropan-1-one with the provided phosphonium ylide.
1 answer:
Answer:
2-methylene propylbenzene
Explanation:
The Wittig Reaction is a reaction that converts aldehydes and ketones into alkenes through reaction with a phosphorus ylide.
The ketone in this case is 1-phenylpropan-1-one. The provided phosphonium ylide is shown in the image attached. The reaction involves;
i) alkylation
ii) addition
The product of the major organic product of the reaction is 2-methylene propylbenzene.
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Answer:
- <em>Brønsted-Lowry acid: HNO₂</em>
- <em>Brønsted-Lowry base: NH₃</em>
- <em>Conjugate acid: NH₄⁺</em>
- <em>Conjugate base: NO₂⁻</em>
Explanation:
The equation is:
<em>Brønsted-Lowry acids</em> are H⁺ donors.
<em>Brønsted-Lowry bases</em> are H⁺ acceptors.
Thus, on the left side, <em>HNO₂</em> is the acid and <em>NH₃ </em>is the base.
The <em>conjugate acids</em> and <em>conjugate bases</em> are on the right side of the equation.
The <em>conjugate acid</em> is the spieces that is formed after a base accepts the proton; thus it is <em>NH₄⁺</em>. A <em>conjugate acid</em> contains one more H atom and one more + charge than the base that formed it.
The <em>conjugate base</em> is the species that is formed after the acid donates its proton; thus, <em>NO₂⁻</em> is the <em>conjugate base</em>. A <em>conjugate base</em> contains one less H atom and one more - charge than the acid that formed it.
Summarizing:
- Brønsted-Lowry acid: HNO₂
- Brønsted-Lowry base: NH₃
- Conjugate acid: NH₄⁺
- Conjugate base: NO₂⁻