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<h3>Organometallic reagent</h3>
Organometallic chemistry is the study of organometallic compounds, which are substances that contain at least one chemical bond between a carbon atom from an organic molecule and a metal. These substances include alkali, alkaline earth, and transition metals, as well as metalloids like boron, silicon, and selenium. In addition to links to organyl fragments or molecules, bonds to 'inorganic' carbon, such as those to carbon monoxide (metal carbonyls), cyanide, or carbide, are also typically regarded as organometallic. Although they are not strictly speaking organometallic compounds, some similar compounds, such as transition metal hydrides and metal phosphine complexes, are frequently included in discussions of such substances. The phrase "metalorganic compound," which is comparable but different, describes molecules that contain metals but do not have direct metal-carbon bonds but do have organic ligands.
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Answer:
Hey buddy, here is your answer. Hope it helps you.
Explanation:
The force stopping the object's motion might be an obvious one - the ground! Friction is a force that slows or stops motion. Friction is the resistance to motion created by two objects rubbing against each other (the sled and the snow, for instance). Even air causes friction.
Answer:
Explanation:
There are few simple rules in organic chemistry which a person must learn.
1. In predicting a structure from ozonolysis, number of oxygen present in products must be counted. In this particular example, there are 2+3+1 = 6 oxygen atoms are present in three molecules. This means that there should be at least three confirmed double bonds must be present in the molecule of Dictyopterene.
2. There are in total of 3+5+3 = 11 carbon atoms present, making 2^11 = 2048 possible structures for this particular structure. But since there are three double bonds present, this will reduce the number of possible structures as well.
3. Questions also says that when fully hydrogenated, the molecule generates Butylcycloheptane. That means that our base molecule is Butylcycloheptane and this molecule contains at least three double bonds.
So, first we draw the molecule of butylcycloheptane. After this, we think of were double bonds could be present. We do have the products. Let's make their structures first. I have also mentioned the possible breakup where the ozonolysis has occured by color code. You can see them in the reference image attached.
Part 1 out of 2: There is only one chiral carbon present in the molecule and have two possible isomers. Cis and Trans. Only one stereogenic carbon is present, that's why two possible isomers. Image attached.
