1. 2. Show how you would synthesize benzylamine from each of these compounds, using the following...
Select the reagents you would use to synthesize the compound below from benzene. (More than one step is required. If no third step is needed, choose (none).) Reagents Available f. KMnO4, H20 g. H2, Pd/C h. SO3, H2SO4 i. NaOH, H2O a. Br2, FeBr3 b. Cl2, FeCl 0 d. CH3CI, AICl3 Br e. CH3COCI, AICl3 N-bromosuccinimide (NBS) ball & stick labels Step 1: Step 2 Step 3
Devise a route to carry out the following conversion: OH (Specify the reagents you would use to carry out the conversion by using letters from the table. The reaction may require more than one step, if so, write the letters in the order that they are used, e.g., hb. If two or more ways of conversion to the same product are possible, show only one of them.) Reagents available a. SOCl2, pyridine e. NaNH / NH3 i. 1. NaNH NHA...
les of reagents to synthesize cach of the following compounds List the reagent(s) in order that will accomplish this transformation, beginning with the number of the starting material. Enter your choices without spaces or punctuation (i.e ledcba). Starting materials C C Н.С OEt EtO OEt 2 Reagents f. EtO Na a. CH Br k. NaOH, H2O b. CH CH Br g. SOC h. NH3 L CH NH HCI, HO, heat I с. Cн,CH,CH,Br d. (CHa)2CHBr e. CH3CH2CH(Br)CH NH(CH) Compound 1:...
[References] How would you synthesize the following compounds from butanoic acid using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Example: ab Reagents PBry I KOH / alcohol 1. NaBHA 2.H,0 KOB b .1. LIAH 2.HO f Mgidry ether HP 1.2. Cul 1.00, 2.,0* PE d 1-bromobutane HBr dark no peroxides NON 1.BH/THF 2 H2O. NaOH pt H.O heat 1 pt 1 pt a) octane g 1 pt...
How would you synthesize the following compound from acetylene and reagents in the table? Choose the most efficient route. Specify reagents using letters from the table, first reagent on the left. Example: ab H H CH3CH2CH2 CH2CH3 a. Br2 b. CH3CH I Reagents available d. CH3 CH2CH2CH2Br g. KOH/ ethanol e. Hy / Lindlar's catalyst | h. NaNH / NH3 f. 1. BHz in THF 2. H2O2 in NaOH c. CH3 CH, CH,Br Reagents (in order of use) are Submit...
Homework 9: Alpha Be sure to answer all parts. Report Synthesize (2)-hept-5-en-2-one from ethyl acetoacetate (CH,COCH Co,Et) and the given starting material. Sol Br Guided (z)-hept-5-en-2-one Draw four organic reaction intermediates, and seleet the single best set of reaction steps. reagents for each of CHCoCH2CO2Et [1] NaOEt, [2] HC-CCH2Br [1 HCL, [21 HC CCH2Br O I1 Mg, 12] HC CCH2Br draw structure 0 H2 (2 equiv), Pd-C H2 (2 equiv), Pd c mCPBA H,SO4 11,0+,a HOCH CH,OH, TSOH LIAIH KMno,...
How would you synthesize the following compounds from botanic acid using reagents from the table? Use letters from the table to list reagents in the order used (first at the left).
Use the provided possible starting materials and reagents to synthesize the target product Target Product 1 step(s) may generate multiple stereoisome OH Ho CH CH CH OH OH OH OH 1. Mix Reactants inDMSOHo HO-P-OH (cold, dilute (heated, concentrated) Na t HOEt, 25 C 1. BH3/THF2. HO-, H202. H2 (excess)Pt or Pd or Ni 1. OsO4, NMO2. NaHSO3 1. LiAlH42. H20. (H+) NaBH4CH3OH 1. KMn04, NaOH2. H30+Na2Cr207H2S04, H20 PCCCH2C12
..) Complete the following transformation using some of the reagents provided below. Show each step of the synthesis and the reagents needed. For extra credit: H+ (cat) HT/H20 Os04 (CH3)2CO CH3CH2Br мСРВА HO-(cat) H2/Pd/lindlar HgSO4 BH3 HOCH2CH2OH Br2 Na/NH3 nBuli KMnO4 NaNH2 CH3(CH2)2CHO Mg/Et20 OH
40. (38) Predict the product or provide reagents needed to complete each transformation. OH A (a-b) K-OH excess OH Na+ HCO3-. (c-d) 1. SOCI 2. NH, OH 1. KOH 2. CH3CH2CH Br a H (e-f) NH 3. NHỊNH H, Hz. Pd ?? ?? (g-h) N3 NH2 NOZ (g-k) -NEN OH CI N 1. CH3 2. Ag20 3. heat 1. CHE 2. Ag20 3. heat (l-m) NH2 ?? NEN OH ?? (n-0) CI CI CI CI (put) 1. Mg, ether 2.Co,...