Part 1: (1] X [2] H20 view structure Select the correct reagent X. There may be more than one correct answer. O CH;-CHMGB a (CH, CH)½CULI O CH;=CHBR O CH;-CHLİ Part 2 out of 2 (1] Y [2] H2O OH Select the correct reagent Y. There may be more than one correct answer. O CH;-CHMgBr O CH; CHLİ CH,-CHBR (CH,-CH),CuLi

20. Which structure is the most basic? A 00: H₂C CH₂ CH₂ B F₂C 00: 'N CH₂ CH₂ с H₂C O CH₂ D F₂C 0 0 CH₂ CF₁ 11/L-

I got 1 - fluro-4, 4-dimethylcyclohexan but it is not correct. Can you oelae help Br H H Cl Enter the correct IUPAC nomenclature. cis-1-bromo Submit Previous Answers Request Answer × Incorrect; Try Again; 2 attempts remaining

4. Are there any RX compounds from part A that are not expected to undergo an Sn1 or Sn2 reaction? Which and why not?

For the substituted cyclohexane compound shown, identify the atoms that are trans to the bromo substituent. I CH3 Br HD HCI- HA HB НОЕ K ČI HG Identify the atoms that are trans to the bromine. A В C D E F G H K

A) Draw the products for the following reactions: CH₂-0- CH 0- CH₂-C 0 (CH₂) 12-CH₂ -CH3 HH??-??-2 ?? -(CH2) 16 (CH2) 16-CH₂

What is the major product of the following reaction? OH Na,CryO,, H,SO,, H,0 Select one: CH:- CH:CH CH: a. CH:0-C- CH:CH CH: Ob. CH:0-C- OCH;CH:CH: Oc. CH C- OCH CH,CH Od. OH CH CH;CH:CH:

OH me for the who H3C- -CH3 H3C CH3 Cr(VI) compounds are common reagents for the oxidation of alcohols. Primary alcohols are oxidized to carboxylic acids and secondary alcohols are oxidized to ketones. The mechanism involves a reaction similar to the E2 elimination, whereby a C-O double bond is formed with a reduced Cr(IV) compound as the leaving group. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions XT H3C-C-CH3 "A: H :0: MON HA ago H3C CH3

O || CH3-CO-C-CH3 tCH3CH2CH, NH CH 3 | CH3-C-CL + CH3-N-CH3 Complete the following reaction.

Complete the next reaction: