From the di ketone compound we prepare the given compound by
using reducing agent it is hydride reduction 
3. Show how you could synthesize 2,4-pentanediol using a hyd ride reduction
Show how you could synthesize the products below using a
Grignard reagent and appropriate electrophile by drawing the
overall balanced equation.
НО не он PhPh.
Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. No mechanisms are required for this question. You do not need to show formation of the Grignard reagent. [2 marks] HO H3COH Ph Phi
Show how you could synthesize 3-pentanol starting with molecules of no more than two (2) carbons.
5. Show how you could synthesize the following. (16 pts) A Using the Wittig reaction y vang Ho wang reason Mo + Phypoger 8 ОН Hint: Use the appropriate aldehyde or ketone, and a Grignard Reagent 6. Write the mechanism for the following reaction. (8 points) OH 1. emger 2. H₂O*
Show how you would synthesize the following acid using carbonation of a Grignard reagent. Show how you would synthesize the following acid using carbonation of a Grignard reagent.
The reaction is
3) Using structural formulae, give balanced equations to illustrate how you could synthesize the following esters, using the same type of reaction that was utilized in this experiment: (i) (ii) (iii) 2-propyl cyclopentylethanoate 2-butyl hexanoate benzyl benzoate (Α.Κ.Α. benzyl benzenecarboxylate)
PLEASE ANSWER ALL OF THE QUESTION (a, b and c)
Show how you could synthesize the following products via a Williamson ether synthesis. Include any reagents that would be necessary for the reaction to occur.
Show how you would synthesize the following 3- amine in good yield
using alcohols of carbons 4 or less as your only source of carbon
CH3 、CH3
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents. (20 pts) A. CH COOH (starting from ortho-nitrotoluene) B. HN (starting from nitrobenzene)
Show how you could synthesize prop-1-yne from: 1. 2-bromopropane 2. Propan-1-ol 3. 1,2-dichloropropane 4. Ethyne Thank you!!!