(a) Interpretation: The products of the given reaction are to be drawn. Concept introduction: The reaction of alcohols with halogen acids ( HX ) is a general method to obtain 1 ο , 2 ο or 3 ο alkyl halides. This method is preferred due to the formation of H 2 O as leaving group. The more substituted alcohols generally react rapidly with halogen acids.
(a) Interpretation: The products of the given reaction are to be drawn. Concept introduction: The reaction of alcohols with halogen acids ( HX ) is a general method to obtain 1 ο , 2 ο or 3 ο alkyl halides. This method is preferred due to the formation of H 2 O as leaving group. The more substituted alcohols generally react rapidly with halogen acids.
Solution Summary: The author explains that the reaction of alcohols with halogen acids (HX) is a general method to obtain alkyl
Definition Definition Organic compounds in which one or more hydrogen atom in an alkane is replaced by a halogen atom (fluorine, chlorine, bromine, or iodine). These are also known as haloalkanes.
Chapter 9, Problem 9.19P
Interpretation Introduction
(a)
Interpretation: The products of the given reaction are to be drawn.
Concept introduction: The reaction of alcohols with halogen acids (HX) is a general method to obtain 1ο,2οor3οalkyl halides. This method is preferred due to the formation of H2O as leaving group. The more substituted alcohols generally react rapidly with halogen acids.
Interpretation Introduction
(b)
Interpretation: The products of the given reaction are to be drawn.
Concept introduction: The reaction of alcohols with halogen acids (HX) is a general method to obtain 1ο,2οor3ο alkyl halides. This method is preferred due to the formation of H2O as leaving group. The more substituted alcohols generally react rapidly with halogen acids.
Interpretation Introduction
(c)
Interpretation: The products of the given reaction are to be drawn.
Concept introduction: The reaction of alcohols with halogen acids (HX) is a general method to obtain 1ο,2οor3ο alkyl halides. This method is preferred due to the formation of H2O as leaving group. The more substituted alcohols generally react rapidly with halogen acids.
If possible, replace an H atom on the
a carbon of the molecule in the
drawing area with a methyl group
substituent, and replace an H atom
on the ẞ carbon with a hydroxyl
group substituent.
If one of the substituents can't be
added for any reason, just don't add
it. If neither substituent can be
added, check the box under the
drawing area.
en
HO
OH
Curved arrows are used to illustrate the flow of electrons. Use
the reaction conditions provided and follow the curved arrows
to draw the intermediate and product of this
hydrohalogenation reaction.
Include all lone pairs and charges as appropriate.
Br
Select to Draw
51°F
Sunny
esc
F1
HBr
Select to Draw
1,2-hydride
shift
Br
Select to Draw
Q Search
F2
F3
F4
1
2
#
#
3
DII
L
F5
F6
F
tA
$
%
Λ
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