can I please get help with these questions? I need the molecules drawn and arrows as well as the products. showing your work will be very helpful. thank you!

1) Complete the following questions for the molecule A: (2E)-1-chloro-4-methyl-pent-2-ene. Include all lone pairs on heteroatoms, charges, or any necessary steps such as deprotonation steps for an alcohol formation. a) Provide the proper line bond diagram of the molecule. Include proper stereochemistry as indicated. b) This molecule undergoes SN1 type reaction. Use arrow pushing to show proper formation of carbocation for molecule B. c) Provide any potential resonance structures available for molecule B. Use proper arrow pushing to indicate the resonance mechanism if available. d) In the presence of water, the molecule B can generate constitutional isomer on a primary, secondary, and tertiary carbons. Show using arrows how you could possibly generate these 3 distinctly different isomers (roview re-arrangement reactions in Organic 1). e) Identify the type of hybridization at each carbon atom using VBT for both molecules (label as sp, sp2, sp3) and provide reasoning. Note the difference at carbon 1 . 1) Provide proper orbitals setup for C2 and C3 for molecule A and C1 for molecule B. Note the difference is at carbon 1. 9) Uso WebMO to draw the structure with proper idealization for structure A and B and indicate if there are any symmetry elements. Note the difference in geometry at carbon 1