As we add dilute NaOH into the given compound, NaOH abstracts proton from the alpha to carbonyl group and forms the different enolates as shown in the given image. Then in dilute acidic conditions, the formed enolates converted into keto group and that time when keto enol tautomerization takes place, that time stereocenters changes to form the more different products as shown in the given image.
Choose the major compounds present after the following ketone is treated with dilute aqueous base. (5...
Choose the major compounds present after the following ketone is treated with dilute aqueous base. NaOH (cat.) H2O ry 1 2. 3 4 ah 6 A. 1 and 2 B. 1 and 3 C. 1 and 4 D. 2 and 5 E. 3 and 6 F. 1, 4, and 6 G. 2, 3, and 5 H. 3, 4, and 5 1. 1, 2, 4, and 5 J. 3, 4, 5 and 6
1) Choose the correct structures for X and Y. 2) The following aldol reaction can produce 4 products. Select the structure that is not a possible product of the following reaction. 3) Choose the major compounds present after the following ketone is treated with dilute aqueous base. 4) Draw the alkyl bromide(s) that is(are) needed to prepare the following ketone using the acetoacetic ester synthesis. O Br LDA TMS-CI CH3-Li Br Х Y -78 °C NEt3 1 2 3 A....
QUESTION 5 OH The Major Product in the reaction sequence below is OH 1) HBO OH 2) KOT-Bu 3) CH3CO3H 1 2 3 @ A4 0 0 B.1 0.2 D.3 QUESTION 6 он The Major Product in the reaction sequence below is он 1) Bra (dilute), H20 CH 2) NaOH 3)H" (cat , H2O OH OH ОН ( با ما - -OH OH Note: All Products Race mic 1 2 A2 E. 1 C. 0.3 QUESTION 11 The Major Product...
5. Which of the following compounds will produce a tertiary alcohol when treated with aqueous acid (H2O, H30*)? all of them none of them А B с D E
Question 2 (1 pt) When treated with aqueous NaOH, the following compounds give an aldol product which then undergoes dehydration to give a new product (with Estereochemistry). Please give structural formulas for both products. + TH + 1 H NaOH NaOH H20 + H₂O H20 Aldol product
3. Which one of the following compounds is present as a pair of stereoisomers? 3-pentanol 4-methylcyclohexanol 2-butyne 2-bromopropane 1-butene А B С D E 4. Which one of the following compounds will not react with HC=CNa? MeBr PhCH Br PhCHCHЬBr PhBr CH.CHBr А B С D E 5. Which of the following compounds will produce a tertiary alcohol when treated with aqueous acid (H2O, H,0")? none of them all of them С B D E
5) Which of the following compounds is hydrolyzed the slowest in aqueous NaOH? І п ш IV у E) II A) III B) I C) IV 6) 6) What is the major product when (CH3)2CHCH2CH2Br undergoes the following reaction sequence: (Step 1) Mg, ether (Step 2) CO2 (Step 3) H30+ A) 4-methyl-1-pentanol B) 2-methyl-2-butanol C) 4-methylpentanoic acid D) 3-methylbutanoic acid 7) Diisobutylaluminum hydride can be used to carry out which of the following conversions? A) aldehyde to carboxylic acid B)...
5. Identify the major product expected to form at the completion of the following synthetic sequence. O OH SO3, H2SO4 Br2 H2O H3O*-H2O но ОН Br ОН Он Он Br о Он Br но но Но НО но Br SO3H Br Br (A) (B) (C) (D) (E) 6.Which of the following synthetic sequences is expected to yield 2-chloro-4-nitrobenzoic acid in highest yleld? 1. KMnO OH Cla- FeCl HNO3- H2SO heat (A) 2. H30 1. KMnO4 , OH HNO- H2SO Clo-...
Which of the following compounds, when treated with sodium nitrite in aqueous hydrochloric acid at room temperature, do not generate nitrogen gas? NHCHa NH2 CH2NH2 N(CH3)2 CH3 3 4 2 A. 2 and 4 only D. 1, 2, and 4 only B. 2 and 3 only E. 2, 3, and 4 only C. 1 and 4 only
I need answer ASAP The major organic product for the following reaction is MgBr 1. (excess) i 2. H2O/H+ mentore veritative OH 1 O 3 O O 4 O 1 The major organic product for the following reaction is LiAIH, Н ОН он он 1 он 2 он 3 4 O2 о 4 о О 3 The major organic product for the following reaction is Bry, FeBrz Br (mono bromination) Br 3 H 1 Br 2 0 3 0 01...