We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN1)?...
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN.)? PhCH,CI Phci (CH),CHCI CHCI Ph CHCI A B D E 4. Which one of the following compounds is optically active (chiral). С D A B
Alkyl Halides and their Reactions: Nucleophilic Substitution and Elimination l. Predict the major organic product for each of the following. (1 major structure is all that needed in each case). (3 points each) Br CH3ONa CH3CH2ONa (for "d", show elimination product only, there will also be some substitution) NaOH e, optically active (for "e", show substitution product or products only. If both enantiomers form, draw both) Is the product solution for reaction "e" above racemic or optically active? (1 point...
Which of the following alkyl halides would react the fastest with H2O in Sn1 reaction? CH3CH2CH2CH2Br, (CH3)2CHCH2Br, CH3CH2CH(CH3)Br, (CH3)3CBr Multiple Choice CH3CH2CH2CH2Br O (CH3)2CHCH2B O CH3CH2CH(CH3)Br O (CH3)3CBI O
5. Which one of the following carbonyl compounds will react faster by nucleophilic attack? (CH3)2CHCHO (CH3)3CCHO (t-Bu),CO (CH3)2CO с D CH3CHO А B 2
3. Complete the following nucleophilic substitution reactions of the alkyl halides below by drawing the structure of the product. 20 pts CHCI + -OH- B. (CHshCCH2l CEC-H C. CH3 H3C D. CH3CI+ OCCH2CH
Which of the alkyl halides below will react the fastest in an SN1 reaction? CH3 CH3 CH3 CH H2C H2C H3C-C-I H-C-Br H3C-C-Br H-C-I CH3 CH3 CH3 CH3 CII-C C-C C-C C-C-IIC
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options would be best suited for a unimolecular nucleophilic substitution reaction? مو لہ کی لہ لا 3. Describe the following reactions in written form, making sure to use the following terms where appropriate: nucleophile, lone pair, loss of leaving group, electron-deficient, and electrophile. . و ». . که ملیہ -- « -
9. Which of the following alkyl halides is most rea order kinetics? y halides is most reactive in an elimination reaction having first- A. A B.B C.C D.D E. E 10. Which of the following statements is (are) true about an E2 elimination reaction? A. It is fastest with 3 halides. B. It exhibits second-order kinetics. C. A better leaving group should make a faster reaction. D. Both (It is fastest with 3 halides) and (It exhibits second order kinetics)...
D obro ontzil 3) c. You subjected the secondary alkyl halides to both Sn2 and Sn1 reaction conditions. By which mechanism did each alkyl halide react faster, SN2 or S17 On the basis of your comparison, what can you conclude about the adu! likelihood of a secondary alkyl halide reacting by one or the other mechanism? Why? ni balb o za
Which one of the following compounds is an acetal? Which one of the following compounds is an acetal? OEt ОН Co ou E A B С D Which one of the following carbonyl compounds will react faster by nucleophilic attack? (CH3)2CHCHO (CH3)3CCHO (t-Bu)2CO CH3CHO A B C D (CH3)2CO E