one of the parents (or both of them) could be a carrier for the allele of light brown skin if the brown skin is the dominant gene. so if both of the parents are carriers of the gene for the light brown skin, then theres a small chance that their child could have light brown skin
Answer:
Hydras are generally sessile, but they can detach and move to another location by gliding slowly on their base. Sometimes they somersault, float, or use their tentacles to move along. ... If cut into several sections, a new Hydra will generate from each piece.
Explanation:
F BLOCK is the block on the period table that contains the actinide series of elements.
Actinide series of elements are two rows under the periodic table which include Lanthanide series and Actinide series. These are all radioactive elements and all of these are not not found in nature. All these are included in F block element.
Answer:
Compound A: 1-bromo-1-methylcyclohexane
Compound B: 1-methylcyclohex-1-ene
Explanation:
In this question, we can start with the <u>I.D.H</u> (<em>hydrogen deficiency index</em>):

In the formula we have 7 carbons, 13 hydrogens, and 1 Br, so:

We have an <u>I.D.H value of one</u>. This indicates that we can have a <u>cyclic structure or a double bond</u>.
We have to keep in mind that the Br atom must be bonded to a t<u>ertiary carbon</u>. <u>We can not have a double bond</u> because in the ozonolysis reaction we have only <u>1 product</u>, therefore, we can not have a double bond in the initial molecule (if we have a double bond in the initial molecule we will have more than 1 product in the ozonolysis reaction).
With this in mind, we will have a <u>cyclic structure</u>. If we have 7 carbons and we need a tertiary alkyl halide. We can have a cyclic structure of 6 members and a methyl group bonded to a carbon that also is bonded to a Br atom <u>(1-bromo-1-methylcyclohexane).</u>
In the reaction with
we will have an <u>elimination reaction</u>. In other words, we have the production of a double bond inside of the cyclic structure <u>(1-methylcyclohex-1-ene)</u>.
See figure 1 for further explanations.
I hope it helps!