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- i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,List the reactivities of the following compounds according to the SN1 reaction. please explain why a) Methyl chloride b) isopropyl chloride c) tertiary butyl chlorideRearrangements can occur during the dehydration of 1° alcohols even though no 1° carbocation is formed—that is, a 1,2-shift occurs as the C— OH2+ bond is broken, forming a more stable 2° or 3° carbocation, as shown in Equation [1]. Using this information, draw a stepwise mechanism for the reaction shown in Equation [2]. We will see another example of this type of rearrangement in Section 16.5C.
- Show the relationship between E2 Reactions and Alkyne Synthesis ?Are these SN1 or SN2 reactions? What is the major product structural form?Assume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final product
- The formation of a carbocation is the rate-determining step for an SN2 reaction. A. True B. FalseList the alkyl halides in order of decreasing reactivity towards the Sn1 reactionIn parts 1 and 2 draw the two organic products of this reaction, showing any nonzero formal charges. Then, in part 3 answer the question regarding purification of the reaction mixture. 1. Draw the product with the higher molecular weight here: 2. Draw the product with the lower molecular weight here:
- What are characteristics of an alkyl group and leaving group in an SN2 reaction? What is their purpose?What is the product of E2 elimination or (3R,4R)-3-chloro-2,2,4-trimethylhexane?(S)-2-Butanol, instead of (R)-2-butanol, is obtained from the reaction between (R)-2-bromobutane with hydroxide ion. What kind of reaction is this (SN1,SN2,E1 OR E2) ? Explain briefly this inversion of configuration (i.e. (R) configuration for the reactant and (S) configuration for the product) and What is this inversion called?