the third one is not E Identify how you would make hexylamine from 1-hexanol: Choose from the following list of reagents: A NaN3 E LAH B NaCN 03 F C H₂, Pt G DMS D PBr3 H H₂O "NH₂
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- select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4Based on Steric Effect and Electron Delocalization Explain: 1. Phenol is not easily attacked by a positive reagent as aniline 2. Solubility of acetylinic compound in may bases Please do answer all question for an upvote!! Thank you!4) Which of these would give a positive iodoform (I2, NaOH) test?
- a. Propose a synthetic pathway for cis-[NiCl2(CO)2] using trans-effect. b. Propose the methods to differentiate the isomers in between [RhCl2(H2O)4]Cl and [RhCl3(H2O)3].H2O.4. What problem(s) might occur if we make the following changes to the work-up procedure of our Ionone synthesis? a) Omit the washing with water before washing with saturated sodium bicarbonate. b) Omit the washing with brine.Draw the products formed when p-methylaniline (p-CH3C6H4NH2) is treated with each reagent.a. HClb. CH3COClc. (CH3CO)2Od. excess CH3Ie. (CH3)2C = Of. CH3COCl, AlCl3g. CH3CO2Hh. NaNO2, HCli. Part (b), then CH3COCl, AlCl3j. CH3CHO, NaBH3CN
- Compound MM (g/mol) ortho mp (oC) meta mp (oC) para mp (oC) Nitroacetanilide 180.16 94 155 214-217 Methyl nitrobenzoate 181.15 -13 78-80 94-96 Based on the table above, determine the regiochemistry of your methyl nitrobenzoate and draw the structure Based on the table above , determine the regiochemistry of your nitroacetanilide and draw the structure.SHOW COMPLETE SOLUTIONS Q3. Which isolate has A260/280 ratio of above 2.0?Draw the product of the reactions of succinic anhydride with each of the listed reagents. Assume in all cases that the reagent is present in excess and an aqueous workup takes place after each reaction. A. Reaction with (CH3)2CHOH. \table[[Select,Draw,Templates More,,],[/,//,I//,H,Erase]] B. Reaction with NH3. \table[[Select,Draw,tes More,Erase],[/,//,III,C,H,N,0]] Question Source: Vollhardt 7e0 Organic Chemistry: Structure And Function Publishęr: W. Freemar C. Reaction with phenylmagnesium bromide in THF, followed by H+,H2o. \table[[Select,Drav,v T,lates,,,Erase],[1,II,III,C,H,0,]] D. Reaction with LiAlH4 in ether, followed by H+,H2O \table[[Select,Draw,Templates More],[/,//,III]] \table[[3,0]] \table[[,2,Q
- Please answer ASAP Draw the arrow-pushing mechanism for the following reaction. 1) P(OCH2CH3)3, NaH 2) 4-Methyl-2-PentanoneThreonine is a naturally occurring amino acid that has two stereogenic centers. a. Draw the four possible stereoisomers using wedges and dashes. b. The naturally occurring amino acid has the 2S, 3R configuration at its OH two stereogenic centers. Which structure does this correspond to?6 I have a NMR spectrum of my synthesized para nitroaniline sample, but it is dilluted. I try to figure out with what. I need a chemdraw from heptane, ethylacetate and ortho nitroaniline.