Answer:
See explanation
Explanation:
The reaction that we are considering here is quite a knotty reaction. It is difficult to decide if the mechanism is actually E1 or E2 since both are equally probable based on the mass of scientific evidence regarding this reaction. However, we can easily assume that the methylenecyclohexane was formed by an E1 mechanism.
Looking at the products, one could convincingly assert that the reaction leading to the formation of the two main products proceeds via an E1 mechanism with the formation of a carbocation intermediate as has been shown in mechanism attached to this answer. Possible rearrangement of the carbocation yields the 3-methylcyclohexene product.
Answer:
It is Likely to Be Sodium (Na) coz as You Down The group the reactivity increase
Explanation:
Lithium diisopropylamide (LDA) is used in many organic synthesis and is a strong base. It is prepared by the acid base reaction of N,N-diisopropylamine ( [(CH₃)₂CH]₂NH ) and butyllithium ( Li⁺⁻CH₂CH₂CH₂CH₃ ).
The equation is show below as:
[(CH₃)₂CH]₂NH + Li⁺⁻CH₂CH₂CH₂CH₃ ⇒ [(CH₃)₂CH]₂N⁻Li⁺ + CH₃CH₂CH₂CH₃
N,N-diisopropylamine ( [(CH₃)₂CH]₂NH ) is a weaker acid and hence, LDA ( [(CH₃)₂CH]₂N⁻Li⁺ ) is stronger base. (Weaker acid has stronger conjugate base)
Butyllithium ( Li⁺⁻CH₂CH₂CH₂CH₃ ) is a very strong base and hence, butane ( CH₃CH₂CH₂CH₃ ) is a very weak acid. (Strong base has weaker conjugate acid)
It condenses when it passes below 212 degrees Celsius, or 100 degrees Fahrenheit