Problem 11-56 Order each of the following sets of compounds concerning SN1 reactivity. Most reactive=1; Least reactive=3. CH3 H3C-C-Cl CH3 (a) CS Scanned with CamScanner H3C CH3 Cl NH 2 1 CH3CH2CHCH3
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- Problem 11-57 Order each of the following sets of compounds concerning SN2 reactivity. Most reactive=1; Least reactive=3. CH3 H3C-C-Cl CH3CH2CH2Cl (a) CH3 CS Scanned with CamScanner Cl CH3CH2CHCH3PROBLEM 4-30 Rank the following radicals in decreasing order of stability. Classify each as primary, second- ary, or tertiary. (a) The isopentyl radical, (CH3)2CHCH₂-CH₂ (d) (b) The 3-methyl-2-butyl radical, CH3-CH-CH(CH3)2 (c) The 2-methyl-2-butyl radical, CH3-C(CH3)CH₂CH3Organic Chemistry 2 - 14.26
- Correct the one that marked wrongPROBLEM 5-21 Which of the following compounds are chiral? Draw each compound in its most symmetric con- formation, star (*) any asymmetric carbon atoms, and draw any mirror planes. Label any meso compounds. You may use Fischer projections if you prefer. (a) meso-2,3-dibromo-2,3-dichlorobutane (b) (±)-2,3-dibromo-2,3-dichlorobutane (c) (2R,3S)-2-bromo-3-chlorobutane (d) (2R,3S)-2,3-dibromobutane (e) (R, R)-2,3-dibromobutane (f) H- HO CHO -OH -H CH₂OH H Br H. CH₂ H CH₂ H Br (h) H Br CH₂ H H CH₂ H Brneed answer fast i'll rate up
- It is not neces Cl NO2 What is the name of the following? 1-chloro-2-nitrobenzene Submit Answer Retry Entire Group 9 more group attemptsPROBLEM 3-25 (a) Draw both chair conformations of cis-1,4-dimethylcyclohexane, and determine which conformer is more stable. (b) Repeat for the trans isomer. (c) Predict which isomer (cis or trans) is more stable.A set of three nucleophilic displacement reactions is shown below: NaN3 CH;OH CH3CH2CHCH3 SN2 reaction A, X = | В, Х%3D Br C, X = OH Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest? Submit Answer Try Another Version 2 item attempts remaining
- What are the missing reagent(s) for the reaction below? (Select all that apply? OH PBr3 A ☐ A C B D 1) ??? 2) NaCN SOCI₂ NEt3 B TSCI NEt3 с с CN HCN DPROBLEM 11-38 Develop syntheses for the following compounds. As starting materials, you may use cyclopentanol, alcohols containing no more than four carbon atoms, and any common reagents and solvents. (a) trans-cyclopentane-1,2-diol (b) 1-chloro-1-ethyleyclopentane f (c) OCH, CH₂ (e) OCH₂CH₂ C-CH₂CH₂ (1) OCH,PROBLEM 3-24 Draw the most stable conformation of: (a) ethylcyclohexane (c) cis-1-tert-butyl-4-isopropylcyclohexane (b) 3-isopropyl-1, 1-dimethylcyclohexane