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![Problem 1. Rank the reactive intermediates by decreasing stabilization, most stable first. (ranking, e.g. like, 1> 2>
3 > 4)?
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Please explain step by step as to how I rate
stability orders for carbocations, carbanions and
free radicals??](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1422a69b-e9fa-4951-8378-322a71ca77be%2F4ec2881a-3660-4f56-bef9-e2168c352df5%2F2lmonv_processed.jpeg&w=3840&q=75)
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- 6. Rank order the following substitution reactions by reaction rate (Fastest to Slowest) OHS structure of DMSO A. || > | > | > IV B. II >> III > IV C. IV > II > | > ||II D. II >> IV > III E. None of the above I || III IV ~ en Br ~ Br CH,NH, CH₂OH CH₂SH DMSO CHÍNH, CH₂OH CH₂OH + Product Product Product ProductS Draw the product of the reaction showing the stereochemistry at any stereogenic centers. **** H [1] H-C=C [2] H₂O draw structure...Draw both resonance structures of the mnost stable carbocation intermediate in the reaction shown +. HBr • You do not have to conside stereochemistry Do not include anionic counter-1ons, e g., I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. in
- 1. what reaction and meachanism is this ? 2. Explain mechanism what happenning in each step on this picture 3. why is it says "stop" when NaOEt added ? does reaction stop there ? why does it stop ? ? what principle ?Which of the following correctly describes a key step of the reaction shown in the box? 1. ELONA 2 2. HаО, НСІ OEt :o: :o: :o: A) Et H3C p: 1 :o: :o: :o: :o: B) H3C Et H3C :o: :o: :0: + C) H2C H3C :o: H :0: :0: :o: D) H3COEt H3C OEt O A O B OD O=Which synthetic route(s) would complete the reaction shown? Br || ||| I and II O I and III ? HO OH + enantiomer Synthesis I: 1. NaCCCH3; 2. Na/NH3(I) ;3. OsO4; 4. NaHSO3, H₂O Synthesis II: 2. NaCCCH3; 2. H2, Lindlar's catalyst; 3. MCPBA; 4. aq. H₂SO4 Synthesis III: 1. NaCCCH3; 2. H₂, Pt; 3. MCPBA; 4. aq. H₂SO4
- [References] Draw the major organic product of the following reaction. CH3CH2CHCH2CH3 SOCI2 OH • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. opy aste C. - [F ChemDoodle Submit Answer Try Another Version 3 item attempts remaining|| Ranking the stability of carbocation V Rank the carbocations in the table below in order of decreasing stability (1 most stable and 4 least stable). (Choose one) 1 - most stable 2 3 4 - least stable Explanation Check + ہے F F (Choose one) Q Search + (Choose one) 3 (Choose one) LEE 0 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | AccessiWhat is the Potential energy diagram for this reaction. Pls draw with as much detail as possible. labels and scale) 2-methylpropan-2-ol ---> 2-methylpropene +H2O Draw the potential energy diagram for the reaction of 2-methylpropan-2-ol ---> 2-methylpropene + H20 (1) Label the structures of the (a) reactants, (b) intermediates, (c) transition states, (d) products, and (e) activation energies (E.) for each step. (2) Which step is the rate-determining step? (3) Identify the electrophile and nucleophile in each step when applicable.
- The DG° (free energy change) for the con... The DG* (free energy change) for the conversion of A to B is predicted to be which of the following? ⒸOH₂ OH step 1 Multiple Choice DG=0 DG 0 H₂O step 2 step 3 Cannot be determined from the Information provided + H-CI1. Reaction mechanism 2. Show sterochemistryeq M Visited [Review Topics] [References] Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. ✪ . You do not have to consider stereochemistry. . Do not include anionic counter-ions, e.g., I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate resonance structures using the symbol from the drop-down menu. 4 Submit Answer 981 *** CH₂ + ChemDoodle HCI Detry Entire Group Show Hint Sn [F 4 more group attempts remaining Previous Email Instructor Next> Save and Exit
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