Construct a three-step synthesis of 3-bromocyclopentene from cyclopentane. Drag the appropriate items into the bins. Note that each bin should hold only one item, and not all reagents and structures will be used. Reagent 3 Reagent 2 Reagent 1 Final product Reactant Step 1 product Step 2 product (cyclopentane) (3-bromocyclopentene) NBS ROOR HBr HBr ROOR Br Br2 Br2 Hzо hv Br Br Br Br Br (CH3)3CO K
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- Construct a three-step synthesis of 3-bromocyclopentene from cyclopentane. Drag the appropriate items into the bins. Note that each bin should hold only one item, and not all reagents and structures will be used.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:Fill in the missing reagents and “key intermediate” in each transformation below:
- Construct an efficient three-step synthesis of 1,2-epoxycyclopentane from bromocyclopentane by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used.Draw the product for the substitution reactions below. Then, draw the proper FULL electron-pushing mechanism for the reaction, including intermediates with lone pairs and formal charges, and all electron pushing arrows (SN1 vs SN2). Label the electrophile and nucleophile in each step.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
- Hi, I need help with this multi-step problem. Using any of these reactions: SN1/SN2, E1/E2, Alkene Additions, Alkyne reactions, or Radical reactions - I need to create a synthesis problem that has a starting material and a targeted product. The product must have at least 9 carbons. The second step is to create an answer key for my synthesis problem which includes 6 steps. (please provide reactants and products for each step and one of the steps must be a radical reaction) And lastly, please provide the mechanism for the radical reaction.An SN2 mechanism takes place when 3-(bromomethyl)pentane is added to each nucleophile listed below. Which nucleophile will also require an acid-base step after the substitution step in order to produce a neutral (not charged) product? A. LiN(CH3)2 B. NaI C. KN3 D. HSCH3 (Please type answer no write by hend)15.5 (mno) Predict the major product or reagent that completes the transformation
- [VI1] Instructions: Provide the missing reagent/s, substrate/s, or product/s for each reaction. (refer to the photo below)The synthesis shown above can be accomplished in three steps. Select the reagents for each step from the dropdown lists below.Classify the following reaction as an Sn1, Sn2, E1, E1cB, E2 reaction. Can you show me the leaving group and explain how to find a leaving group? And how to identify the other reactions?