Answer:
<h2>Actin and myosin.</h2>
Explanation:
The cells that allow your bones to move, the movement of thick (myosin) and thin (actin) filaments during contraction
.
During a contraction thick and thin filaments do not shorten but increase their overlap of each other.
Thin filaments slide past thick filaments extending more deeply into the A band.
The I bands and H bands decrease in lenght as Z discs are come closer together
.
Sarcomere represents area between two Z disc, so the sarcomere gets smaller during a contraction
.
The answer to this is 22, confirmed by gradpoint
Explanation:
A clastic sedimentary rock is a rock that is formed from pre-existing rock materials and minerals. This materials have been transported to their new positions by the agents of denudation.
- Clastic sedimentary rocks are made up of rock fragments predominantly.
- The matrix is usually remnants of other rocks.
- A cementing material can form between clasts and holds them in place. Cements are usually iron oxides, calcite e.t.c.
- These rock types are usually formed from mechanincal weathering of rocks
- Mechanical weathering breaks down rocks into chunks.
- Examples are breccia, conglomerates, e.t.c.
Learn more:
Sedimentary rocks brainly.com/question/2740663
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Answer:
The answer is

Explanation:
The energy of a quantum of light can be found by using the formula
<h3>E = hf</h3>
where
E is the energy
f is the frequency
h is the Planck's constant which is
6.626 × 10-³⁴ Js
From the question
f = 4.31 × 10¹⁴ Hz
We have
E = 4.31 × 10¹⁴ × 6.626 × 10-³⁴
We have the final answer as

Hope this helps you
Answer:
See explanation below
Explanation:
You are not providing the starting material, however, I manage to find a similar question to this, so I'm gonna use it as a basis to help you answer yours.
Now let's analyze what is happening in the reaction so we can predict the final product.
We have a ketone here, reacting at first with LDA. This is a very strong base that is commonly used in reactions with ketones and aldehydes to promove a condensation. To do this, as LDA is a strong base it will occur firts an acid base reaction, substracting the most acidic hydrogen in the molecule (Which in this case, is the Beta hydrogen of the carbonile). This will cause an enolate formation.
Then, this enolate will react with the CH3I and form a new product. The final result would be a ketone with a methyl group now attached. In the picture 2, you have the mechanism and final product.
Hope this helps