Working Backwards Parte Deux. a.First, identify which functional groups changed during the reaction. Did stereochemistry change too? b. Based on your answers to A and B, what kind of reaction occurred here, SN1 or SN2? c.Suggest reagents and solvent that could accomplish this reaction.

2-butanol (CH,CHOHCH,CH,) is classified as a(n). A. Choose the best reagents to complete the reaction shown below. C. primary alcohol secondary alcohol tertiary alcohol ether 10 What type of functionality does phenol contain besides the aromatic ring? B. D. Bean beeties can infest a pantry supply of dried beans. To control the beetles romone traps are used to attract the insects. Choose the best reagents to complete the following reaction in the synthesis of the dried bean beatle sex pheromone C amino alkene hydroxy ° alkyl E aldehyde с D 1.H B 20 A PB DMF E. Rank the compounds (shown below) in order of increasing acidity. на 20 F. P 500 pyridine PC DMF Br Choose the reagents that would be most likely to completion 818 A |<< B << C |<<\ D TTTTT D. Is an incorrect answer << |<<

In an E2 reaction, what are the characteristics of a good base?  How does a chemist tell a strong versus weak or bulky versus not bulky nucleophile? What is the best type of solvent for this reaction? Please define the terms.

17. a. Label the reactive features, highlight the most reactive one, then highlight what it needs. Also, state if the reaction will start to create a carbocation, carbon radical, or carbanion, or will cause loss of aromatic character. If a carbocation, carbon radical, or carbanion starts to develop, label where that will occur. CH3 with Cl, and FeCl, CH2 CH3 b. Use mechanism arrows to illustrate the reaction that occurs. c. If applicable, use stabilization resources to deal with the carbocation, carbon radical, or carbanion that starts to develop during the reaction, and draw the structure of any resonance-stabilized intermediate. d. Continue labeling and diagramming the reaction until you find the major stable product(s). e. Finally, state the stereochemistry of the major product(s) and use either Fisher projection or perspective formula representations to illustrate that stereochemistry.

Fill in the blanks in the following SN2 reactions with either the appropriate nucleophile,electrophile, or product and include any stereochemistry where it is relevant.

help;  the reactions are all covered in Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise. Chapter 15-17

help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working