Biology, Pages 58-67 |
From inside the book
Results 1-2 of 2
Page 29
In the ball - and - stick models shown in Figure 4.7c , the middle carbon is called
an asymmetric c carbon because it is attached to four different atoms or groups of
atoms . The four groups can be arranged in space about the asymmetric carbon ...
In the ball - and - stick models shown in Figure 4.7c , the middle carbon is called
an asymmetric c carbon because it is attached to four different atoms or groups of
atoms . The four groups can be arranged in space about the asymmetric carbon ...
Page 50
... a . structural isomers b . geometric isomers c . enantiomers d . isotopes 6.
Identify the asymmetric carbon in this molecule : OH H H H il a lb lo la Te C - C -
C - C - C - H H H H H H 7. Which functional group is not present in this molecule
50.
... a . structural isomers b . geometric isomers c . enantiomers d . isotopes 6.
Identify the asymmetric carbon in this molecule : OH H H H il a lb lo la Te C - C -
C - C - C - H H H H H H 7. Which functional group is not present in this molecule
50.
What people are saying - Write a review
We haven't found any reviews in the usual places.
Other editions - View all
Common terms and phrases
acid Activity addition adenosine amino animal Appendix arise arrangement asymmetric attached basis biological body branch called carbon and hydrogen carbon atom carbon compounds carbon dioxide carbon skeleton carboxyl cell Chapter characteristic chemical complex components Concept contains covalent bonds cyanate Determine dissolve distinctive diversity double bonds drug early Earth effective electrons elements enantiomers energy example fat molecules female Figure force foundation four fuel functional groups geometric isomers groups of atoms hydrocarbons hydrogen hydroxyl Important inorganic joined L-Dopa laboratory learned living matter living organisms major male molecular architecture nitrogen organic chemistry organic compounds organic molecules origin oxygen Parkinson's disease patients phosphate phosphate group possible present produce properties Proteins release rings shape share shell shows single skeletons of organic structural formula structural isomers study of carbon sulfhydryl synthesis term thalidomide urea valence variations versatility vitalism Wöhler