B - False. The crystals have the same internal arrangement of atoms in the same species. For example, all crystals of quartz (Onion, Amethyst, Citrine, Smoky) have the same trigonometrical arrangement.
the atoms in salt (NaCl) are arranged in a cubic way.
Answer:
Order zero
Explanation:
Let's consider the decomposition of ammonia to nitrogen and hydrogen on a tungsten filament at 800°C.
2 NH₃(g) → N₂(g) + 3 H₂(g)
The generic rate law is:
rate = k × [NH₃]ⁿ
where,
rate: reaction rate
k: rate constant
n: reaction order
When n = 0, we get:
rate = k × [NH₃]⁰ = k
As we can see, when the reaction order with respect to ammonia is zero, the reaction rate is independent of the concentration of ammonia.
Answer:
Speed and acceleration
Explanation:
i would say this bc the formula is related to acceleration if you looking at all the possible exceptions im not a expert in this range but im just giving you what i would pick so if you get it wrong im sorry lol.
At its discovery, benzene was recognized to be a unique unsaturated hydrocarbon because it either failed to react, by substitution with common reagents or reacted by addition that led to reactions with alkenes.
<h3>What are unsaturated hydrocarbons?</h3>
Unsaturated hydrocarbons are the hydrocarbons which have at least on double or triple carbon to carbon bond in its molecules.
All other hydrocarbons are unsaturated except for the alkanes and the cyclic alkanes.
Benzene is an aromatic compound which has a special six-carbon ring with are resonance structure reflecting the presence of three carbon-carbon bonds in its molecules.
The common reactions of unsaturated hydrocarbons are substitution and addition reactions.
However, benzene on its discovery did not undergo any of these reactions.
In conclusion, benzene showed a difference when compared with the common unsaturated hydrocarbons as it did not undergo either substitution or addition reactions.
Learn more about benzene at: brainly.com/question/6028840
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Answer: .B. 13C NMR spectra display peaks for only carbons that bear hydrogen atoms.
Explanation:
The statements that are true about 13C NMR are:
A. In 13C proton-decoupled NMR spectra, all peaks are singlets.
C 13C NMR chemical shifts occur over a greater range than 1H NMR chemical shifts.
D. 13C NMR easily differentiates between the different hybridized carbons (sp3, sp2, and sp hybridized carbons).organic-chemistry
Therefore, the option that isn't true is option B. "13C NMR spectra display peaks for only carbons that bear hydrogen atoms". This is false because 13C NMR will show every peak in the spectrum and it doesn't matter if it's only carbons that bear hydrogen atoms as everything will be shown.
