Answer:
CH₃CH(CH₃)CH(C₃H₇)CH₂CH(CH₃)₂:
4-isopropyl-2-methylpentane.
Explanation:
Step One: Draw the structure formula of this compound. Parentheses in the formula indicate substitute groups that are connected to the carbon atom to the left.
For example, the first (CH₃) indicates that the second carbon atom from the left is connected to:
- the CH₃- on the left-hand side,
- the -CH(C₃H₇)CH₂CH(CH₃)₂ on the right-hand side,
- a hydrogen atom, and
- an additional CH₃- group that replaced one hydrogen atom.
Each carbon atom in this compound is connected to four other atoms. All bonds between carbon atoms are single bonds.
The C₃H₇ in the second pair of parentheses is the condensed form of CH₃CH₂CH₂-. See the first sketch attached. Groups in parentheses are highlighted.
Step Two: Find the carbon backbone. The backbone of a hydrocarbon is the longest chain of carbon atoms that runs through the compound. See the second sketch attached. The backbone of this compound consists of seven carbon atoms and is highlighted in green. The name for this backbone shall be heptane.
Step Three: Identify and name the substitute groups.
The two substitute groups are circled in blue in the second sketch.
- The one on the right -CH₃ is a methyl group.
- The one on the left is branched.
This group can be formed by removing one hydrogen from the central carbon atom in propane. The name for this group is isopropyl.
Step Four: Number the atoms.
Isopropyl shall be placed before methyl. Start from the right end to minimize the index number on all substitute groups. The methyl group is on carbon number two and the isopropyl group on carbon number four. Hence the name:
4-isopropyl-2-methylheptane.
Anything can be broken down, as long as it is not as small as an atom
Answer:
Military
Explanation:
I may be wrong but military seems most likely
Answer: No.
Explanation: One mole of zinc is not the same as one atom of zinc. In one mole of zinc, there are approximately 6.022*10^23 atoms of zinc.
Answer:
See explanation below
Explanation:
The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.
Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.
First, all what we have here is an acid base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.
In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.
See picture 2, for mechanism