Answer:
See explanation
Explanation:
In this case, we have to remember the meaning of the nomenclature "18:2Δ9,12". Where 18 is the <u>number of carbon atom</u>s, 2 is the <u>number of double bonds,</u> and the numbers successive to Δ "delta" the position of the double bonds <u>starting</u> to count from the carboxylic -COOH end of the molecule.
In other words, the main functional group is a <u>carboxylic acid</u>. We have a total of 18 carbons. Additionally, we have 2 double bonds. On carbons 9 and 12.
Lets see figure 1
I hope it helps!
Because its only representing the most stable isotope of that element but its considered the atomic mass and not average atomic mass
Hi!
The answer is breathing.
Protozoans are organisms that can multiply themselves in humans, and serious infections can develop from one organism. The most frequently transmission methods are contaminated food or fecal contact. Dog bites inoculate bacteria into deep tissue, and they also serve as a transmission method.
Breathing is not considered to be likely to transmit protozoan infection because protozoans rarely develop in the respiratory tract.
This reaction would give rise to two products.
- 2-bromo-3-methylhexane, and
- 3-bromo-3-methylhexane.
However, 2-bromo-3-methylhexane would be more common than 3-bromo-3-methylhexane among the products.
The hydrogen atom in a hydrogen bromide molecule carries a partial positive charge. It is attracted to the double bond region with a high electron density. The hydrogen-bromine bond breaks when HBr gets too close to a double bond to produces a proton and a bromide ion .
The proton would attack the double bond to produce a carbocation. It could attach itself to either the second or the third carbon atom.
Carbocations are unstable and might decompose over time. The first carbocation is more stable than the second for having three alkyl groups- i.e., straight carbon chains- attached to the center of the positive charge. Alkyl groups have stabilizing positive induction effect on positively-charged carbon. The second carbocation has only two, and is therefore not as stable. The first carbocation thus has the greatest chance to react with a bromide ion to produce a stable halocarbon.
Bromide ions are negatively charged. They attach themselves to carbocations at the center of positive charge. Adding a bromide ion to the first carbocation would produce 3-bromo-3-methylhexane whereas adding to the second produces 2-bromo-3-methylhexane.
The <em>most likely</em> product of this reaction is therefore 3-bromo-3-methylhexane.