around the age of two they might start to kinda ''leave''(or venture) there parents
Tap water and rain water are both homogeneous, even though they may have different levels of dissolved minerals and gases. A bottle of alcohol is a man-made homogeneous mixture, from a fine Italian wine to a glass of Scotch whisky. In the human body, blood plasma is an example of a homogeneous mixture.
Answer:
91383 J
Explanation:
The equation of the reaction can be represented as:
------>
Given that:
The standard enthalpy of formation of NO(g) is 91.3 kJ⋅mol−1 at 298.15 K.
The equation below shown the reaction between the enthalpy of reaction at a particular temperature to another.
= 
where:
= enthalpy of reaction
= the difference in the heat capacities of the products and the reactants.
∴
= 
= ![1(91300 J.mol^{-1} ) +\int\limits^{435}_{298.15} [{(29.86)-\frac{1}{2}(29.38)-\frac{1}{2}29.13}]J.K^{-1}.mol^{-1} \, dT'](https://tex.z-dn.net/?f=1%2891300%20J.mol%5E%7B-1%7D%20%29%20%2B%5Cint%5Climits%5E%7B435%7D_%7B298.15%7D%20%5B%7B%2829.86%29-%5Cfrac%7B1%7D%7B2%7D%2829.38%29-%5Cfrac%7B1%7D%7B2%7D29.13%7D%5DJ.K%5E%7B-1%7D.mol%5E%7B-1%7D%20%5C%2C%20dT%27)
= 91300 J + (0.605 J.K⁻¹)(435-298.15)K
= 91382.79 J
≅ 91383 J
Answer:
if its a neutral atom there should be 6 electrons because there are 6 protons
Explanation:
Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.
Discussion:
1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.
2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.
3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.
4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.
Learn more about carbonyl here:
brainly.com/question/21440134
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