Aktiv Learning App Cengage Digital Learning Part of Speech Table for Assign x o Mail-Karen Ento-Outlook * + app.aktiv.com Your Aktiv Learning trial expires on 02/06/25 at 01:15 PM Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Problem 17 of 30 Drawing Arrows heat 4 O M B D 5x H H Und Settings H Done :0: H Jar
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- Please draw the Lewis structure Dont leave NO2 or MeO Draw them out tyCurved arrows are used to illustrate the flow of eletrons. Follow the arrows to predict the product of this reaction. Include all lone pairs and ignore inorganic byproducts.01:50 4G File Details 4CH003/UM1: Fundamentals of... Introduction NaBH4 OH C=0 H benzophenone diphenylmethanol Ketones are readily reduced to secondary alcohols by reaction with sodium borohydride. The aim of this experiment is to determine the time required to effect the complete conversion of the ketone, benzophenone to diphenylmethanol at room temperature. This investigation may be achieved by isolating and analyzing the reaction product after different reduction times. Infrared spectroscopy affords a convenient method of analysis; by comparing the IR spectrum of the crude reaction product at different time intervals one would expect to see the intensity of the hydroxyl absorption peak increase relative to that of the original carbonyl peak. From this you can deduce the optimum time for the reduction process at room temperature. Procedure Note the "reduction time" that the demonstrator assigns to your group. Different groups will be assigned different times, eithert = 2.5 minutes,…
- REACTIONS OF HYDROCARBONS Professor has assigned the analysis of unknown hydrocarbon samples to Eoteng Mabutiogting based on their reaction profile. The summary of the observed reactions are tabulated below along with the possible structures of the samples. Identify each unknown sample by matching the respective reactionprofle with the given structures. Name each structures then briefly explain the reason for your answer. Sample Brz in CCl. (dark) Brz in CCl. (light) KMNO4 in NaOH AGNO. in NH: Fading of reddish- Fading of reddish- Brown precipitates Silver precipitates brown color brown color No reaction Fading of reddish- No reaction No reaction 2 brown color Fading of reddish- Fading of reddish- Brown precipitates No reaction brown color brown color H3C. CH3 CH3 CH3 H;C H3C `CH3 H3C Sample Identity and Rationalization 1 2Choices for PDT1 and PDT2 are CLA, RIS, KUL, LET, PIE, No ReactionMasteringChemistry: CHE154 X Ce session.masteringchemistry.com/myct/itemView?assignmentProblemID=144673376&offset3Dnext CHE154-H Gen Chem II Bronikowski S20||| Report - Google Docs X Explanation APPLICATIONS OF SUBSTITUTION AND ELIMINATION Predicting the products of nucleophilic epoxide ring opening A www-awu.aleks.com/alekscgi/x/lsl.exe/10_u-IgNslkr7j8P3jH-li... Add the necessary reaction conditions above or below the arrow in this organic reaction. Also, if a major product is missing from the right-hand side, draw it in. Ilm ALEKS Check ***|||| C $ C + T 32 X ALEKS - Tiffany Te-L-P X Q III... Q 9 A Mon Nov Cl C OH 2/5 + D 2022 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy CenterAktiv Chemistry ← → C https://canvas.tamu... Jobs For Aggies - H... app.101edu.co 76°F Mostly cloudy Success Confirmation of Question X Draw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore byproducts. CI Jobs - Zoo Jobs Ne... heat CH3ONA, CH3OH + Internships | Job Ca... internship paper Your Online Accoun... Question 7 of 21 99+ Urban Wildlife Infor... A Site Suitability An... Please select a drawing or reagent from the question area Aktiv Learning Submit X 10/31/2022 : 4:09 PM sI need help with this question (Not honor class) (Not grading)Aktiv Chemistry ← → C https://canvas.tamu... Jobs For Aggies - H... app.101edu.co 76°F Mostly cloudy Success Confirmation of Question X Draw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore byproducts. Br H₂O Jobs - Zoo Jobs Ne... heat + Internships | Job Ca... internship paper Your Online Accoun... Question 6 of 21 99+ Urban Wildlife Infor... A Site Suitability An... Please select a drawing or reagent from the question area Aktiv Learning Submit X 10/31/2022 : 4:06 PM sQUESTION- Label these spectra attached. Use them to discuss differences in reactant and product spectra that determine/support positive product formation. please no general responses, be specific to peaks in the spectra attached. EXPERIMENT: Synthesis of Benzil - Multi-Step Synthesis Part B ReferencesLehman, J.W. Operational Organic Chemistry: A Problem- Solving Approach to the LaboratoryCourse, 3 rd Ed., Prentice-Hall, Inc: New Jersey, 1999, p. 449.C0% (b) HO, HCI Exercise 2 Diazonium ions (R-N2") are such powerful leaving groups that they offer a method for generati primary carbocations (Na gas is the leaving group). Interestingly, hydrolysis (solvolysis with water) any of the indicated diazonium ions (below) gives the same three products in exactly the same rati Provide a mechanism for these reactions consistent with this data. (Hint: Think about a commc intermediate for all the reactions.) OH HO. 48 48 4 Exercise 3 For the indicated atoms in each molecule, determine if they are homotopic. enantiotopic, diastereotopic or heterotopicSEE MORE QUESTIONS