Identify the benzylic carbons in each of the following structures. (Click on an atom to select...
Identify the benzylic carbons in each of the following structures. (Click on an atom to select it. Selected atoms will turn green. If you make a mistake, click on the atom again to deselect it.)
Homework Answers
A benzylic carbon is a sp3 carbon. The first carbon directly attached to the benzene ring or other aromatic ring is called benzylic carbon.
The benzylic carbon is a saturated carbon that is directly attached to the benzene ring. It is in contrast to the phenyl carbon.
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Identify the benzylic carbons in each of the following
structures. (Click on an atom to select...
Identify the benzylic carbons in each of the following structures. (Click on an atom to select...
Identify the benzylic carbons in each of the following structures. (Click on an atom to select it. Selected atoms will turn green. If you make a mistake, click on the atom again to deselect it.)
Identify the allylic carbons in each of the following structures. (Click on an atom to select...
Identify the allylic carbons in each of
the following structures. (Click on an atom to select it. Selected
atoms will turn green. If you make a mistake, click on the atom
again to deselect it.)
Must provide a clear drawing Identify the allylic carbons in each of the following structures. (Click...
Must provide a clear drawing
Identify the allylic carbons in each of the following structures. (Click on an atom to select it. Selected atoms will turn green. If you make a mistake, click on the atom again to deselect it) An allylic carbon is a carbon adjacent to a double bond. Be careful to select only the carbon atoms and not the bonds.
Select the appropriate reagent for each step of the following synthesis in which propionyl chloride is...
Select the appropriate reagent for each step of the following synthesis in which propionyl chloride is made with a carbon-13 isotope in position 2, starting with 13CO2. (The 13C atoms are shown in a green color). Identify which carbon atom in each intermediate would be labeled by clicking on the atom until it turns green. (If you make a mistake, click on the atom again to turn it back to black. Be careful not to select a bond or an...
Select the specified atoms in each molecule below. Click on an atom to select it, turning...
Select the specified atoms in each molecule below. Click on an atom to select it, turning it green. Be sure to select only atoms, not bonds. ck on an atom to select it; a selected symbol will turn green.
Select the atoms drawn with valid Lewis dot structures. Click on a structure to select it;...
Select the atoms drawn with valid Lewis dot structures. Click on a structure to select it; a selected symbol will turn green.
Highlight - by clicking on - the chirality center(s), if any, in each structure.
Highlight - by clicking on - the chirality center(s), if any, in
each structure. A selected atom will turn green. Click again to
deselect your choice.
Select all of the asymmetric carbon atoms in the following structure. A selected atom will turn...
Select all of the asymmetric carbon atoms in the following
structure. A selected atom will turn green.
Select all of the asymmetric carbon atoms in the following structure. A selected atom will turn green.
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will...
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will turn green. Indicate whether each compound contains a plane of symmetry (internal mirror plane) or not.
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will...
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will turn green. Indicate whether each compound is chiral and the number of stereocenters (see Hint) in each molecule achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters
Identify the benzylic carbons in each of the following structures. (Click on an atom to select it. Selected atoms will turn green. If you make a mistake, click on the atom again to deselect it.)
Identify the allylic carbons in each of
the following structures. (Click on an atom to select it. Selected
atoms will turn green. If you make a mistake, click on the atom
again to deselect it.)
Must provide a clear drawing
Identify the allylic carbons in each of the following structures. (Click on an atom to select it. Selected atoms will turn green. If you make a mistake, click on the atom again to deselect it) An allylic carbon is a carbon adjacent to a double bond. Be careful to select only the carbon atoms and not the bonds.
Select the appropriate reagent for each step of the following synthesis in which propionyl chloride is made with a carbon-13 isotope in position 2, starting with 13CO2. (The 13C atoms are shown in a green color). Identify which carbon atom in each intermediate would be labeled by clicking on the atom until it turns green. (If you make a mistake, click on the atom again to turn it back to black. Be careful not to select a bond or an...
Select the specified atoms in each molecule below. Click on an atom to select it, turning it green. Be sure to select only atoms, not bonds. ck on an atom to select it; a selected symbol will turn green.
Select the atoms drawn with valid Lewis dot structures. Click on a structure to select it; a selected symbol will turn green.
Highlight - by clicking on - the chirality center(s), if any, in
each structure. A selected atom will turn green. Click again to
deselect your choice.
Select all of the asymmetric carbon atoms in the following
structure. A selected atom will turn green.
Select all of the asymmetric carbon atoms in the following structure. A selected atom will turn green.
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will turn green. Indicate whether each compound contains a plane of symmetry (internal mirror plane) or not.
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will turn green. Indicate whether each compound is chiral and the number of stereocenters (see Hint) in each molecule achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters
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