This problem is based on the concept of allylic carbon atom.
An allylic carbon is the carbon which is present adjacent to a carbon-carbon double bond that is a carbon atom bonded to another carbon atom which in turn is doubly bonded to another carbon atom.
Allylic bonds are often weaker and therefore more easily broken. The stability of the allylic radical can be utilised in the preparation of Allylic halides. Allylic halides readily undergo substitution reactions via either unimolecular nucleophilic substitution pathway or bimolecular nucleophilic substitution pathway.
Part a
In the given compound, highlighted atoms are allylic carbons. The representation of allylic carbons is given below:
[Part b]
In the given compound, highlighted atoms are allylic carbons. The representation of allylic carbons is given below:
Ans: Part aThe representation of allylic carbons is given below:
Part bThe representation of allylic carbons is given below:
Identify the allylic carbons in each of the following structures. (Click on an atom to select...
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.
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 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.)
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