Answer:
The answer is IONIC BOND
Explanation:
Steroidogenic acute regulatory, (StAR) protein is a type of globular protein, which allows it act as an active catalyst on substrates. Because the substrates on which enzymes act usually have higher molecular weights of several hundred as compared to the enzymes, only a fraction of the enzyme's surface is in contact with the substrate. This region of contact called the <em>active site</em>, is as a result of the protein folding itself into a tertiary structure.
Once the correct substrate has bound at the active site of the enzyme, an enzyme-substrate complex is created. The substrate is usually held in the complex by combinations of electrical attraction, hydrophobic repulsion, or hydrogen bonding between and from the amino acid; the strongest of which is the ionic/electrostatic bonding due to larger amount of ionic "R" groups in the protein structure.
So whilst all these inter-molecular interactions are possible, the strongest would be <u>ionic bond.</u>
The half-life of the reaction is 50 minutes
Data;
- Time = 43 minutes
- Type of reaction = first order
- Amount of Completion = 45%
<h3>Reaction Constant</h3>
Let the initial concentration of the reaction be X
The reactant left = (1 - 0.45) X = 0.55 X = X
For a first order reaction
<h3>Half Life </h3>
The half-life of a reaction is said to be the time required for the initial amount of the reactant to reach half it's original size.
Substitute the values
The half-life of the reaction is 50 minutes
Learn more on half-life of a first order reaction here;
brainly.com/question/14936355
Answer:molten iron
Explanation:releases heat and light into surroundings
Addition of water to an alkyne gives a keto‑enol tautomer product and that is the product changed into 2-pentanone, then the alkyne need to had been 1-pentyne. 2-pentyne might have given a combination of 2- and 3-pentanone.
<h3>
What is the keto-enol means in tautomer?</h3>
They carries a carbonyl bond even as enol implies the presence of a double bond and a hydroxyl group. The keto-enol tautomerization equilibrium is depending on stabilization elements of each the keto tautomer and the enol tautomer.
- The enol that could provide 2-pentanone might had been pent-1- en - 2 -ol. Because an equilibrium favors the ketone so greatly, equilibrium isn't an excellent description.
- If the ketone have been handled with bromine, little response might be visible because the enol content material might be too low.
- If a catalyst have been delivered, NaOH for example, then formation of the enolate of pent-1-en - 2 - ol might shape and react with bromine.
- This might finally provide a bromoform product. Under acidic conditions, the enol might desire formation of the greater substituted enol constant with alkene stability.
Is there any more to the picture?
