In given reaction primary amine is converted into imine by foemation of C=N bond.
aldehyde or ketone react with primary amine to form imines via C=N bond.
so option b and d are neglected which are alcohols.
to get this product, primary amine reacts with propanal.
Thus option e (propanal/H2SO4) is correct.
option a is incorrect, because with a, we get imine in which carbon of C=N contains 2 methyl gropus which is different from the product.
option c is incorrect, because with option c, we get imine which contain 1 methyl group at C of C=N, which is different from product.
NH2 Select one: O a. propanone / H,804 o b. 2-propanol/ H,SO4 o c. ethanal/ H,...
21, please help. i dont understand at all. B. propanal c. ethanal D. ethanal E. propanone 1 eq 1,2-ethanediol 2 eq ethanol 1 eq 1,2-ethanediol 2 eq methanol 21. Which reactants will make the target product? Target product ? trace HA ANH ave. 22. In which of these reactions does adding acid catalyst not speed up the reaction? (Reagents left off for you to determine.)
Question 21 Provide the reagents necessary to carry out the following conversion. 2-propanol H2SO4 propanal H2SO4 propanone H2SO4 1-propanol H2SO4 Ethanal H SO.
Question 15 Identify each of the following structural formulas as: 0 11 CH3-C-H O 11 CH3-C-CH3 A. MCH3-O-CH2-CH3 A. Propanal B. dimethyl ketone (propanone) C. ethanal D. Ethyl methyl ether 0 11 CH3-CH2-C-H
Which of the following aldehydes does 2-methylbutarial propanal dergo aldol reactions ethanal methanal d Select one: a a b.d ob d.
cdn.inst-fs-lad-prod.inscloudgate.net a) constitutional isomers c) stereoisomers b) cis-trans isomers d) none of these 45) There are 3 functional groups present on this molecule. Name them: HOCH, a) aromatic c) ketone b) alcohol d) aldehyde 46) The name for this molecule is _? a) ethanone c) ethanol CH3-C-H b) ethanal d) ethanoic acid 47) The name for this molecule is_? Н-С-ОН a) methanone c) methanol b) methanal d) methanoic acid 48) The name for this molecule is_? HC -CH, a) propanone...
HO form Which of the following compounds is most reactive towards hudleophilic addition rxns? a) lo i isla ally e) ye • The first step of nucleophilic acyl substitutions I attack of a carbonyl group to intermediate a) electrophilic trigonal c) electrophilic, tetrahedral b) nucleophilic trigonal. d) nucleophilic, tetrahedral Provide the necessary reagents to carry out the Kollowing conversson. a) 1. (CH₃)₂ Culi 2. H₂O b) l. excess DIBAHZ. H₂O ~оси, c)l. excess CH ₂ Mg Br 2. H₂O d)...
select the appropriate structures for A B C and D Brz HNO3 حواء H₂ •Pd/c H₂SO4 Alcz B с A. B C Structure Bank NO2 CI СІ NO2 В 'N NO2 NO2 CI NHL NH ci NO 1 2 3 4 5 7 8
1. CHCOCI. AICI: 2. NH3, H+ b. C. d e. none of these answers NH2 NH2
I Parta A. -OH D. —NH2 B. o oro E. – SH c. o -C-0-H Which two functional groups shown in the figure are present in all amino acids? O C and D OB and D O A and B O C and E O A and D
Alcohol Starting Materials 1. methanol 2. ethanol 3.1-propanol TT 4.2-propanol S. cyclohexanol Reagents available LIAIH f.PBrs b. H,SO4 g.CrOa, H2SO, H,O a. k. CH3CH3 CH2: then H, O L Ce Hs MgBr (phenylmagnesium bromide); then H, O (CH,)2 CHMgBr: then H3O" c. HCl h. NaH m. d. HBr i. CHaMgBr; then H,O n. Dess-Martin periodinane (DMP) e. SOCl j.CH, CHa MgBr: then H,O Write the number letters of the alchol/reagents in the boxes below Alcohol starting material Reagent for step...