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- In the formal SN1 mechanism, the reaction has two steps; however, in reality ____________ steps are actually needed to produce the final product. 3 5 2 4 1Rank the following from most reactive to least reactive in an SN1 reaction.C6H8O7 + 3NaHCO3 -> Na3C6H5O7 + 3H2O + 3CO2 what type of this reaction? Please answer with explanation. Please answer correct will give you upvote.
- 1 example for organic rearrangement reaction show: a. the overall reaction (reactants --> products) b. the reaction mechanism (indicate intermediate product) c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?) d. overall description of the reaction eg., radical substitution or SRCan you make sure to include what the reactions follow SN1, SN2, SNi etcBelow is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?
- For 10.29, the trans product (major product) and the cis product (third product) are displayed as possible E2 products. However, for 10.30, only the trans product (major product) is shown. How come the cis product is not needed?Not sure if Im doing this correctly. Is this an E1 reaction that has a product that has a carbocation or is the product an alkene. can someone explain?The second page is an example how it suppose to be done. (Hex-4-en-3-one+CH3CH2MgBR). It's complete. Please follow directions.