/hich of the following is a step in the mechanism of the following reaction? R-C OH + CНЗОН R-C-OCH3 + H20 Select one: |3| R-C-OH + CH30H R-C OH OH R-C-OH + СНЗОН R-C-OH H-0-CH3 Ob. R-C-OH + CH3OH R-C-OH Oc. HOCH3 OH %3D R-C-OH + CH30 R-C-OH bons Od. OCH 3 R-C-OH + CH30 R-C-OH OCH 3
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- (R)-2-chloropentane was reacted with NaSCH3. The compound yielded 65% (S)-2-chloropentane with the enantiomer making up the other 35%. Which mechanism was followed in the reaction? Both, more SN2 Both, more SN1 SN1 SN2Which of the following bases can remove a proton from a terminal alkyne in a reaction that favors products? CH3O− NH3 CH3C-H2 H2=C-H F-Hello 9. Propose a mechanism for the following reaction. H₂CRO4, H₂SO4 OH
- Which of the following reactions result in a positive ∆ Ssys? a. H2O(g) = H2O(l) b. H2(g) + I2(g) = 2 Hl(g) c. C2H2O2(g) = 2CO(g) + H2(g) d. H2O(g) + CO2 (g) = H2CO3(aq)Select the necessary reagent(s) for the following transformation. a. I2 b. H2/Pt c. Cu^2+ d. H+/H2O e. NaOH f. K2Cr2O7Draw the favored product(s) of the following reactions (organic chemistry)
- 13.30c3 Add curved arrow(s) to draw step 3 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step.a) Provide the major product for the following reaction? noijosen erit mon bonot ed iliw lorlools torW bisnene novio erit bris enonstudoloyo to mains sem erit wsib of been ob uoY Striegsen SO3, H₂SO4 ? + ? THT 10 gad b) Draw the mechanism to obtain the major product.The following reaction has a ΔSsystem < 0 O2(g) → 2O(g) T or F can you explain why this is false?
- Consider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:The base-promoted rearrangement of an a-haloketone to a carboxylic acid, known as the Favorskii rearrangement, is illustrated by the conversion of 2-chlorocyclohexanone to cyclopentanecarboxylic acid. Jo Han Sow La NaOH, THF O Nat H3O+ OH NaOH, THF The mechanism involves the following 5 steps: -ō cyclopropanone intermediate 1. Abstraction of a proton to form enolate anion 1; 2. Formation of a cyclopropanone intermediate 2 with expulsion of chloride ion; 3. Addition of hydroxide ion to form tetrahedral intermediate 3; 4. Collapse of the tetrahedral intermediate and breakage of the three-membered ring to form carbanion intermediate 4; 5. Proton transfer to form the rearranged carboxylic acid. For the following reaction, draw the reaction out on paper, and then draw the structure of cyclopropanone intermediate 2 in the window. 1. NaOH, THF 2. H3O* OHThese reagents can produce ketones with alkynes A. BH3, THF, H2O2 B. KMnO4 C. O3 D. H2SO4, H2O, HgSO4 choices:A,DB,CA,B,CA,B,C,D