Answer to Question #128800 in Organic Chemistry for Kamli Ramli

Organic Chemistry

Question #128800

Give reterosynthesis and synthesis reaction of (E)-pent-3-en-2-one.

Expert's answer

E-butenoyl chloride and grignard reagent like CH₃MgBr react and to form

E-pent-3-en-2-one.

This is the synthesis and reterosynthesis of corresponding compound.

Learn more about our help with Assignments: Organic Chemistry

Comments

No comments. Be the first!

Leave a comment

Related Questions

1. Give reterosynthesis and synthesis reaction of ((isopentyloxy)methyl)benzene.
2. Which of the following statements regarding enantiomers is not true? A) All (+) enantiomers are levo
3. 8. Which compounds above (I-IV) form a set of stereoisomers? A) I, II and III B) II, III and IV C)
4. 9. Which compound would show optical activity? A) cis 1, 4- dimethylcyclohexane B) trans 1, 4- dime
5. 13. (2R, 4S) –2, 4–Dichloropentane and (2S, 4R)-2, 4-dichloropentane are: A) Enantiomers B) Dia
6. 15. Which of the following is/are optically inactive? A) Every achiral compound B) A racemic mix
7. alkane X has molecular formula C4H10. X reacts with Cl2 gas in the presence of sunlight to produce