Answer:
Water would not be able to transport nutrients -‐-‐ in plants, or in our bodies -‐-‐ nor to dissolve and transport waste products out of our bodies. ... Cohesiveness, adhesiveness, and surface tension: would decrease because without the +/-‐ polarity, water would not form hydrogen bonds between H20 molecules.
Review and Study Material Before Going to
Class.
Seek Understanding.
Take Good Notes.
Practice Daily.
Take Advantage of Lab Time.
Use Flashcards.
Use Study Groups.
Break Large Tasks Into Smaller Ones.
Answer:
Explanation:
Stereoisomers are two or more atoms that have the same bonding order of atoms but there is a difference spatial arrangement of the atoms in space.
A plane of symmetry divides a molecule into two equal halves.
A chiral stereoisomer are not superimposed on a mirror image , Hence they do not posses a plane of symmetry.
As a result to that. these non-superimposable mirror images are said to be Enantiomers.
However, a Fischer Projection emanates from a two - dimensional figure which is used for presenting a three - dimensional organic molecules.
From the given question;
Fischer projection for an enantiomer of 2-bromo-2,3-dihydroxypropanal with the bromine oriented horizontally to the left and the hydroxide group oriented horizontally to the right.
we can sketch the way the enantiomer of 2-bromo-2,3-dihydroxypropanal can be seen like the one shown below:
CH₂OH
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Br -------------|----------------OH
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CHO
The objective of this question is to drawn the perspective formula of the molecule.
So , from the attached file below; we can see the perspective formula of the molecule in a well structured 3-D format.
Answer:
Axial
Explanation:
In the most stable conformation of Cis-3-tert-Butylcyclohexanol, the tert-butyl group is at equatorial position and the alcohol group is in the axial position.
If the tert-butyl group is placed in equatorial position, repulsions are minimized. The bulkier the group, the greater the energy difference between the axial and equatorial conformers. Hence for a ring having a bulky substituent, such bulky substituent is better placed in the equatorial position.
The energy difference between the conformers of Cis-3-tert-Butylcyclohexanol is so high that the compound is almost "frozen" in a conformation where the tert-butyl groups are equatorial and the -OH groups are axial. This conformer is more stable by 24 KJ/mol.