CHEM 120 Final Answers - Shshhsjssjjwjsjsvshs

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Which is/are optically inactive? CH,CH, -OH H CH3 H OH H- H. CH3 OH, OH H- HO CH3 CH3 CH3 I II III I and II Il only IIl only Il and III А. В. С. D. O B O A O D

I need help completing this I just need the formula and names of each box, there are some that I did.

× Your answer is incorrect. Which structural formulas represent trans isomers of 1,4-dimethylcyclohexane? H. CH3 | IV ||| | CH3 eTextbook and Media Save for Later CH 3 H || H CH3 CH3- H ||| = CH3 H H CH3 IV CH3 H Attempts: 1 of 3 used Submit Answer

help  please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working

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A. Senyawa diatas termasuk amina primer/sekunder/tersier? Berikan alasan yang tepat! B. Selesaikan dan lengkapi reaksi tersebut!

This question has multiple parts. Work all the parts to get the most points. a Draw the structures of the aldehydes or ketones and alcohols formed when these acetals are treated with aqueous acid and hydrolyzed. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate structures with + signs from the drop-down menu. ChemDoodle

Answer all of questions with explanation please

caq1 Please help with Organic Chemistry question. Thank you

t pt pt pt [References] Draw the structural formula(s) for the branched constitutional isomer(s) with the molecular formula C7H16 that have two methyl groups on the same carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. & Submit Answer ChemDoodle htActivity.do?locator-assignment-take Try Another Version [F 3 item attempts remaining WEB 48 all 41) One Touch Web Access Without Booting Up 7:11 PM 6/29/2022 D P = Other Bookmarks

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help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working

Write the systematic name of each organic molecule: CH3 CH3 O || || structure CH- CH3 OH | CH-CH₂- OH CH₂ CH₂-OH || CH3 CH₂ - CH-C-CH3 CH3 name 0

Name the following compounds. I just need part CC and DD.

S (CQCL3) t σ 200 180 160 140 120 100 80 20 PPM 0 S (CDC13) 9 200 180 160 140 120 100 80 60 40 20 PPM 0 NH₂ T OH .OH །ཚིགས་.. OH

Be sure to answer all parts. Name the following molecular compounds: (a) NI3 (select) v (select) ♥ | (select) (b) F2O7 |(select) v| (select) v (select) v| (select)

||| = O PRINCIPLES OF ORGANIC CHEMISTRY Identifying rigid parts of an acyclic organic molecule In the actual molecule of which this is a Lewis structure, which of the labeled distances can change? H marked O G: F H B C H A N. unmarked G с N O H 0,0.... List all the distances that can change. For example, suppose all the distances were measured at a certain time, and again 0.1s later. If distance A might be 50% bigger or smaller the second time, but all the other distances are certain to be the same, you should write "A". If A and B might be different the second time, but no other distances, you would write "A, B". And so on. Note for advanced students: you can assume the molecule is dissolved in an appropriate solvent at room temperature. X 0/5 You can click the "unmarked" tab to see the molecule without any of the distances marked. S Jacari V 18 CO olo Ar

[1] { [[2]H₂SO] [3]Br2 но C C 32. Br [1] KOH [2] H2SO4 [3] Br₂, H₂O

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Calculus Preface (?) Brytwave Blackboard Quizlet Clutch E Knowledge Check Question 9 Black Forest Biologicals, a biotech startup, has a promising Alzheimer's drug candidate Compound SLT-88 entering Phase I trials this year. SLT-88 is the only product formed by the reaction of two precursor compounds A and B, both of which are quite expensive. The chief medicinal chemist of Black Forest is trying out different reaction conditions to minimize the cost of manufacturing SLT-88. In the table below are listed the initial and final amounts of A and B used under two different trial conditions, and also the actual amount of SLT-88 recovered in each case. Complete the table by calculating the theoretical yield of SLT-88 and the percent yield of SLT-88. Round your amounts to the nearest milligram and your percentages to the nearest whole percent. amount of A amount of B yield of SLT-88 Trial initial final initial final theoretical actual 1000. mg 0 mg 550. mg 286. mg 999. mg 150. mg 0 mg 1000. mg…

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V. 1) Na, NH3 (I) H3C-C=C-CH3 2) D2, Pd/C

Namanclature of the given compound

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