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Answered 1 days After Mar 03, 2021

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Riyanka answered on Mar 05 2021
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DOC022621-02262021131934.pdf
CHEM 2131 - EXAM 1
02126/2021
NAME (print)
NAME (signature)
Problem 1 Problem 2
Problem 3
Problem 4
Problem 5
EXTRA CREDIT
TOTAL
    1     Basics
a) Give an example for a Lewis acid-base reaction, relying on an example that does employ a Lewis acid that is NOT a Bronsted acid. Use curved the a
ow depiction to complement your chemical equation.
) DMSO (1) and acetone (2) are used frequently as solvents in organic chemistry.
They appear to be very similar, yet their structures are quite different. Predict (i.e., draw) their co
ect 3D structures and determine the hy
idization on each atom center.
    0    C)
I-IBC
c) What is the formal energy cost to "rotate" a double bond? Demonstrate the rotation in an o
ital image scheme!
Problem 2     points]    Nomenclature
a) Give the IUPAC names for the depicted compounds
11
) The given names below are inco
ect. Give the co
ect name for each of these compounds:
· 2-methyl-3-tert.-butylpentane
        2-methyl-3-isopropyl-4-chloropentane
· trans-I -pentyl-3-neopentyl-cyclobutane
    3     - (Cyclo)alkanes + Conformational Analysis I
a) Depict an energy diagram that co
elates ring strain with ring size. Clearly mark the different categories of rings discussed in class and for each category mark the most...
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