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- What product is obtained from the reaction of each of the following alcohols with a. H2CrO4? b. HOCl? c. the regents required for a Swern oxidation? 1. 3-pentanol 2. 1-pentanol 3. 2-methyl-2-pentanol 4. 2,4-hexanediol 5. cyclohexanol 6. 1,4-butanediolhelp me draw the products when ethyl isopropyl ether is treated with the following reagent: 1.HBr (2 equivalents) 2.HI (in excess)Can you please check my answer for the following ochem question regarding the enols the the y-diketone CH3COCH2C(CH3)2COCH2CH3 can form. Thank you!
- 3) Which one(s) of the following is/are an acetal ?Which reagent(s) would accomplish the following reaction? 1) LiAlH4 and 2) H2O 1) CH3MgBr and 2) H2O H2O, H+ NaH NaOH, H2ODraw the structure of the product that is formed whent he compound 3-hydroxycyclohexanone undergoes a reaction with 1 equivalent of CH3MgI and then is treated with water. So normally the CH3 would attach and break the double bond with the O but this isn't the correct answer.
- What products would you expect from the oxidation of thefollowing compounds with (i) CrO3 in aqueous acid? (ii) withPCC?(a) tert-butanol(b) cyclohexanol(c) cyclohexanoneDraw the product formed when pentanal (CH3CH2CH2CH2CHO) is treatedwith following reagent. With some reagents, no reaction occurs. [1] C6H5Li; [2] H2OWhat are the major products obtained when the following ether is heated with one equivalent of HI?
- Acetal product formation is difficult, since hemiacetals are stable while acetals are not stable. True FalseWill the bonding of the Zn2+ ion to the ketone oxygen lone pair make the ketone C=O easier or more difficult to reduce? WhySOCl2 (thionyl chloride) converts alcohols into alkyl chlorides. Explain How ?
