O Macmillan Learning 5 % Chapter 6 HW - General, Organic, and Biological Chemistry for Health Sciences - Achie Complete the reaction. Add hydrogen atoms to the appropriate atoms. CH3-CH2-C-N-CH3 H OCT <6 O. + H H Resources ? Hint Submit An Select Draw Templates More /// C H N о SMI ZA MacBook Pro & 7 * 8 ( 9 0 Q2Q A Erase B
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- X app.101edu.co # 3 E UL Week 7: Panopto DII 0 F3 $ R F4 X UL LTU 7-1A Identify the best conditions to complete the SN2 reaction shown below. H % 5 T N3 گیا QL FS A 6 Y Question 18 of 24 40 X F6 & 7 C|Chegg.com U F7 8 A) CH3I, THF B) NaCN, DMSO C) NaN3, ethylamine D) KI, THF X + E) NaN3, DMF PrtScn FB Home ( 9 F9 O ) End 0 & 3 ENG F10 P PgUp - F11 Tp S <10) 1 PgDn D + 6:16 PM 10/18/2022 F12ugen.wileyplus.com/edugen/student/ aintr.uni Klein, Organic Chemistry, 3e actice Assignment Gradebook ORION Downloadable eTextbook gnment Give the major organic product of the following reaction. :O + HN (CH3)2CHI H30+ ? heat OH y.3:20 PM Thu Mar 23 ← Problem 30 of 23 cat. H2SO4 Draw the product of the reaction shown below. Ignore inorganic byproducts. HNO3 (1 equiv) Select to Draw @ : 47% Q Submit <
- Please help solve.0 ning > 3 (Co a = achieve.macmillanlearning.com Chapter 6 HW - General, Organic, and Biological Chemistry for Health Sciences - Π Resources ? Hint Subm boXylitol, which is used as a sugar substitute, is produced by the reduction of D-xylose. Modify the molecule to show the product of the reaction. You may need to add or remove atoms or bonds. © Macmillan Learning к $ O H C H-C-OH H₂ HO-C-H H-C-OH CH₂OH D-xylose OCT 11 % de Lemistry Y cloudy 2 W app.101edu.co 12 3 E UL 7: Panopto PII $ 4 R X F4 Identify the best conditions to complete the SN2 reaction shown below. H % 5 UL LTU 7-1A T Br F5 6 X Question 10 of 24 Y F6 C|Chegg.com & 7 U F7 A) CH3I, THF B) HBr, THF C) KI, H₂O D) KI, THF x + E) CHI, CH3OH PrtScn 8 FB Home ( 9 A & S ENG End ) 12 ☆ 0 F10 P Tp PgUp S * F11 0 C Sub 6:13 10/18/20 PgDn =(CH₂)₂CHCH₂OC-OCH₂CH₂ MAR 28 R F V 5 T G Search or type URL G B H₂SO4 H₂O 6 tv ♫ Y H N og & Reaction C MacBook Pro 7 Select Draw Templates / ||| ||| 3 U Reaction D C Select IN ★ 00 * 8 M Draw A I C 0 → K H ali ZA Templates More ( 9 More < O ) -O L command - P A. Q2Q option Aa [ +1 21 Frace = Erase } 1 deleNernst equation for pair IO3 |I': RT E = E° + nF In a(10;)a°(H*) a(I¯) RT a(IO;)a(H") E = E° + nF a(I") RT E = E° –- nF In a(IO; )a°(H*) a(I¯) nF a(IO,)a°(H*) lg RT E = E° + a(I¯)If oxymercuration reactions are anti additions, how come one of these examples looks like anti, and the other one looks like syn? Would someone be able to draw out both mechanisms?NBS heat Draw the molecule(s) on the canvas by choosing buttons from the Tools (for bonds and charges), A toolbars. H± 12D EXP. CONT. H C N O S F CI Br Br P F × Incorrect; Try Again; 2 attempts remaining Note that, in the second propagation step, bromine is attacked by the least sterically hindered carbon ra Δ A. Submit Previous Answers Request Answer5-52 The following syntheses have flaws in them. What is wrong with each? (a) .CH3 .CO2H 1. Cl2, FeCl3 2. KMNO4 CI (b) CІ CI. 1. (CH3)3CCI, AICI3 2. KMNO4, H2O CO2HQuestion 4 of 14 Write the structure of the products formed in the following acyl group transfer reactions. Identify the reagents as esterifications or thioesterifications. E D с 7 28 R F 7 V 96 OH 5 C Search or type URL T G catalyst B Siv 6 Y MacBook Pro H Draw the major organic product of reaction A. Draw nonbonding electron pairs where applicable. Select Draw Templates More N ///// S U J 8 M CH TEZAO 9 I K H < 0 ✓ O *** L O command P A. T **** option Q2Q 74 { [ ? Aa I +1 "1 Erase 1 delete return shiftSEE MORE QUESTIONS