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- Rank the following carbocations from least to most stable. h ||| A) || < |||<1 B) III < | <1 C) ||| < | < || D) | < || < |||3. For the following structures: CH3a C-CH,CH3 C Hy' H (a) Determine whether each radical is a primary, secondary, or tertiary radical. (b) Rank these radicals in terms of their relative stability (1 = most stable to 3 = least stable). 4 Draw the (2) banoggata 1o||| O STEREOCHEMISTRY Identifying the enantiomer of a simple organic molecule ander Coen Stractare in the table that is an Chianciom CHICER the tabl H CI ****** Br Explanation ay Molecule 1 BL CI Br H 0 Molecule 4 ****** H Br CI Onone of the above Check 1019 Molecule 2 Br H Cl 0 Molecule 5 Br ""H CI OCT 4 WITC Molecule 3 HO CI tv ♫ ***** Molecule 6 Br H hone *** CI H Br Tent ore, CHECK the home X OF CHIC 5 0/5 DOX Under Olivia Ⓒ2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | A TAO
- Which of the following represents allylic carbocation? CH, - CH = CH, CH3 - CH = C - CH3 CH3 - CH- CH = CH2 II III 1 & III -b & ||COa) Draw and label the possible stereochemistry (R/S) of all potential products from cis and trans addition of chlorine to the double bond of cis-2-butene. (Hint see Expt. 3) Clearly indicate meso, enantiomer and diastereomer relationships. CH3 H CH3 CH3 CH3 X- H H cis trans tr H ||||| H *Predict the product for the following reaction. H₂C A I and II HH3C xoxoxox B D IV E cis-1-bromo-3-methylcyclohexane ||| SH H₂C NASH III acetone Br H3C ||||SH IV H
- Give IUPAC name for H3C-HC- C-CH3 | || CH3 OConsider the given alkene below. Identify the products from the reaction of the alkene with the following reagents: Reagent Product Cl₂ in H₂O Cold dilute neutral KMnO4 Hg(OAc)2/THF then NaBH4, NaOH Drag the correct markers to their respective boxes based on the choices from the table below. I HO I HO IV CI ||||||||||IV|| V VI CI II V OH OH НО. X III НО, VI OH OHQ4 * 1,3-thiazolo[4,5,b]pyrdine 1,5-thiazolo[4,5,b]pyrdine 1,3-thiazol[4,5,c]pyridzine 6-thiabicyclo[4.5]decane 1-thia[5.6]decane Both are wrong Q5* ΟΟΟ Q6 * 2H-1,3-oxazete 4H-1,3-oxazete 2H-1,3-oxazane 4H-1,3-oxazane
- Br Based on the intermediate shown below, predict the preferred regiochemistry of this reaction. H₂O H₂O OH Br I Br 11 OH A) I B) II +Starting from the wedge-and-dash structure below (sighting down the indicated bond), rotate the back carbon to provide the structure in the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. H CI K H H3C |||| Drawing < |||| Q Atoms, Bonds and Rings Charges Tap a node to see suggestions. H H H H H Undo X Reset Remove Done RotateFor each solute, click the button under the better solvent. solute Which is the better solvent? (CH,CH,),N :0: :0: NH — С — Nн, CH,-C CH, CH;OH CaCl2 CCI4 CH,OH NaCl I Don't Know Submit