Give a complete curved arrow.pushing mechanism for this reaction, and... 1) Add non-bonding electrons and C-H bonds to the line-angle structures as required. 2) Indicate the Lewis acid/Lewis base (LA, LB) at each step as appropriate, and whether they are also Brønsted acids/bases (LA/BA, LB,BB) 3) GIVE THE NUMBER OF STEPS IN YOUR MECHANISM To preview the image click here :O: H OMe 1- H-AI-H H Excess LiAlH4 :0: L + Lit TOMe
Ionic Equilibrium
Chemical equilibrium and ionic equilibrium are two major concepts in chemistry. Ionic equilibrium deals with the equilibrium involved in an ionization process while chemical equilibrium deals with the equilibrium during a chemical change. Ionic equilibrium is established between the ions and unionized species in a system. Understanding the concept of ionic equilibrium is very important to answer the questions related to certain chemical reactions in chemistry.
Arrhenius Acid
Arrhenius acid act as a good electrolyte as it dissociates to its respective ions in the aqueous solutions. Keeping it similar to the general acid properties, Arrhenius acid also neutralizes bases and turns litmus paper into red.
Bronsted Lowry Base In Inorganic Chemistry
Bronsted-Lowry base in inorganic chemistry is any chemical substance that can accept a proton from the other chemical substance it is reacting with.

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A Lewis acid is a species that accepts electrons. It is positively charged or has vacant orbitals to accept electrons.
A Lewis base donates electrons. It is having negative charge or lone pair of electrons to donate.
A bronsted lowry acid donates protons while a bronsted lowry base accepts protons.
LiAlH4 is a very strong reducing agent, used to reduce almost all carbonyl derivatives. With ester it reacts to give corresponding alcohol, One equivalent of LiAlH4 can reduce two equivalents of ester. Aprotic solvents are required to carry out these reactions.
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