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- 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:Please help me with drawing following reaction steps.. Hydroboration 1-Hexene + (Diethyl ether as solvent + and BH3) -> Hexanol Alkene Bromination 2-Butene (Diethyl ether solvent ) + Br -> anti 2,3 Dibromo butaneI need help understanding the mechanisms and products for this reaction:CH3CH(CH2CH3)Cl + KOH, CH3CH2OH, (20%H2O) ------ >
- draw 2 potential mechanisms for the etherification of ethyl vanillyl alcohol (3-ethoxy-4-hydroxybenzyl alcohol) with methanol and acid (Amberlyst® 15 resin): Sn1 and Sn2, complete with structures and arrows.one of the reaction mechanisms above involves a resonance stabilized carbocation. Draw all resonance structures for this carbocation.1. Using a Lewis acid, BF3, (+) aureal (1) undergoes a rearrangement Org. Lett 2012, 14, 4710-4713. Using arrows propose a mechanism for this rearrangement. 2. Explain why we added BF3 as an acid to the alcohol? How does it help with reaction ( 3 --> 4)? 3. What is the process’ name for (4) --> (5)? 4. going from (5) to (6)? 5. from (6) to (2)?Match the questions with the correct descriptions below: Sn2, E2 E1cb Sn1, E1 (anti) E2, E1cb Sn1, E1 2 steps poor leaving group 2 carbons removed from a carbonyl group carbanion intermediate 3°>allylic, benzylic>2°>1°>CH₃ carbocation intermediate Ist order reaction (r=k[RX]) H-X anti no intermediate 2nd order reaction (r=k[RX][Nu]) polar aprotic solvent
- The following series of reaction steps will yield __________. 1) But-1-yne plus NaNH2; 2) the product of Step 1 plus Butanone; 3) followed by H3O+ 3-methyl-hept-4-yne-3-ol formic acid, propanal and butan-2-ol an octane-based compound containing both a ketone and an alkyne CO2, propanoic acid and buta-1,2-dione 4-methyl-hept-4-yne-1-olCan you draw out the following reaction mechanism: 1. Benzyl alcohol + H2SO4 → Benzyl oxonium ion + HSO4- 2. Benzyl oxonium ion + CrO3 → Chromate ester 3. Chromate ester → Benzylic carbocation 4. Benzylic carbocation + H2O → Benzaldehyde + H3O+ 5. Benzyl alcohol + H2CrO4 → Benzaldehyde + Cr3+ + 3H2SO4 Byproduct: CrO3 + 3 H2O --> Cr3+ + 3 H2SO4Please help me with drawing following reaction steps.. Hydroboration 1-Hexene + (Diethyl ether as solvent + and BH3) -> Hexan Alkene Bromination 2-Butene (Diethyl ether solvent ) + Br -> anti 2,3 Dibromo butane oltane
- When S-2-bromobutane reacts with hydroxide ions (OH-) it forms R-2-butanol. The accepted reaction mechanism of this reaction is shown below. This is an SN2 mechanism.What steps are needed to prepare phenylacetylene, C6H5C = CH, from each compound: (a) C6H5CH2CHBr2; (b) C6H5CHBrCH3; (c) C6H5CH2CH2OH?For the following question please: 1. Predict the products: 2. Give the correct mechanism via correct arrow pushing, and arrow formalisms: 3. Name each mechanism 4. Name each MAJOR and MINOR products: (1R, 2S)-1-iodo-2-methylcyclohexane + KN3 /DMF