I dont know the answer pls help me

Chemistry

1 answer:

Alisiya [41]3 years ago

3 0

Answer:

Unicellular

Explanation:

Unicellular organisms are made up of only a single cell

You might be interested in

Please help if you can !

iogann1982 [59]

Answer:

7630

Explanation:

8 0

3 years ago

Read 2 more answers

Consider the electron configuration. mc011-1.jpg mc011-2.jpg mc011-3.jpgmc011-4.jpgmc011-5.jpg mc011-6.jpg mc011-7.jpgmc011-8.jp

zepelin [54]

The element which has the electronic configuration is CHLORINE.
The atomic number of chlorine is 17 and it has 7 valence electrons in its outermost shell. Because it needs only one more electrons to have a stable octet, it usually react with metals from group one of the periodic table who are normally willing to donate the single electrons in their outermost shells. The ground state electronic configuration of chlorine atom is 1S^2 2S^2 2P^6 3S^2 3P^5.

5 0

3 years ago

Read 2 more answers

stbank, Question 075 Get help answering Molecular Drawing questions. Compound A, C6H12 reacts with HBr/ROOR to give compound B,

Law Incorporation [45]

Answer:

Explanation:

In this case we want to know the structures of A (C6H12), B (C6H13Br) and C (C6H14).

A and C reacts with two differents reagents and conditions, however both of them gives the same product.

Let's analyze each reaction.

First, C6H12 has the general formula of an alkene or cycloalkane. However, when we look at the reagents, which are HBr in ROOR, and the final product, we can see that this is an adition reaction where the H and Br were added to a molecule, therefore we can conclude that the initial reactant is an alkene. Now, what happens next? A is reacting with HBr. In general terms when we have an adition of a molecule to a reactant like HBr (Adding electrophyle and nucleophyle) this kind of reactions follows the markonikov's rule that states that the hydrogen will go to the carbon with more hydrogens, and the nucleophyle will go to the carbon with less hydrogen (Atom that can be stabilized with charge). But in this case, we have something else and is the use of the ROOR, this is a peroxide so, instead of follow the markonikov rule, it will do the opposite, the hydrogen to the more substituted carbon and the bromine to the carbon with more hydrogens. This is called the antimarkonikov rule. Picture attached show the possible structure for A. The alkene would have to be the 1-hexene.

Now in the second case we have C, reacting with bromine in light to give also B. C has the formula C6H14 which is the formula for an alkane and once again we are having an adition reaction. In this case, conditions are given to do an adition reaction in an alkane. bromine in presence of light promoves the adition of the bromine to the molecule of alkane. In this case it can go to the carbon with more hydrogen or less hydrogens, but it will prefer the carbon with more hydrogens. In this case would be the terminal hydrogens of the molecules. In this case, it will form product B again. the alkane here would be the hexane. See picture for structures.