The sites of Lewis basicity in uracil base or sites that undergo hydrogen bonding has to be determined. Concept introduction: Lewis definition: A Lewis acid is a substance that can accept and share an electron pair. A Lewis base is a substance that can donate and share an electron pair. Lewis basicity refers to the ability of the molecule to share the electron pairs on its atomic sites (which are electron rich). Electronegative atom (like nitrogen, oxygen, and fluorine) can also participate in hydrogen bonding by sharing the electron pair with a hydrogen atom which has a partial positive charge. An electrostatic interaction occurs between electronegative atom which is partially negatively charged and a hydrogen atom which is partially positively charged.
The sites of Lewis basicity in uracil base or sites that undergo hydrogen bonding has to be determined. Concept introduction: Lewis definition: A Lewis acid is a substance that can accept and share an electron pair. A Lewis base is a substance that can donate and share an electron pair. Lewis basicity refers to the ability of the molecule to share the electron pairs on its atomic sites (which are electron rich). Electronegative atom (like nitrogen, oxygen, and fluorine) can also participate in hydrogen bonding by sharing the electron pair with a hydrogen atom which has a partial positive charge. An electrostatic interaction occurs between electronegative atom which is partially negatively charged and a hydrogen atom which is partially positively charged.
Solution Summary: The author explains that Lewis acid is a substance that can accept and share electron pairs on its atomic sites. Electronegative atoms can also participate in hydrogen bonding by sharing electrons with hydrogen.
The sites of Lewis basicity in uracil base or sites that undergo hydrogen bonding has to be determined.
Concept introduction:
Lewis definition:
A Lewis acid is a substance that can accept and share an electron pair.
A Lewis base is a substance that can donate and share an electron pair.
Lewis basicity refers to the ability of the molecule to share the electron pairs on its atomic sites (which are electron rich).
Electronegative atom (like nitrogen, oxygen, and fluorine) can also participate in hydrogen bonding by sharing the electron pair with a hydrogen atom which has a partial positive charge.
An electrostatic interaction occurs between electronegative atom which is partially negatively charged and a hydrogen atom which is partially positively charged.
Complete the reaction in the drawing area below by adding the major products to the right-hand side.
If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead.
Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule
to represent each pair of enantiomers, using line bonds at the chiral center.
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No reaction.
my
ㄖˋ
+
1. Na O Me
Click and drag to start
drawing a structure.
2. H
+
Predict the intermediate 1 and final product 2 of this organic reaction:
NaOMe
H+
+
1
2
H
H
work up
You can draw 1 and 2 in any arrangement you like.
Note: if either 1 or 2 consists of a pair of enantiomers, just draw one structure using line bonds instead of 3D (dash and wedge) bonds at the chiral center.
Click and drag to start drawing a structure.
X
$
dm
Predict the major products of this organic reaction:
1. NaH (20°C)
2. CH3Br
?
Some notes:
• Draw only the major product, or products. You can draw them in any arrangement you like.
• Be sure to use wedge and dash bonds where necessary, for example to distinguish between major products that are enantiomers.
• If there are no products, just check the box under the drawing area.
No reaction.
Click and drag to start drawing a structure.
G
Cr
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