Answer:
90% to 97% pure tungsten in a matrix of nickel and copper or nickel and iron.
Explanation:
Heavy metal tungsten alloys are 90% to 97% pure tungsten in a matrix of nickel and copper or nickel and iron. The addition of these alloying elements improves both the ductility and machinability of these alloys over non-alloyed tungsten.
Aqua regia is an oxidative mixture that is highly corrosive and is composed of hydrochloric acid and nitric acid. The Ea (rev) for the reaction is 3 kJ.
<h3>What is activation energy?</h3>
The activation energy is the minimum required energy by the reactant to undergo changes to form the product. The activation energy of the reverse reaction is given by the difference in the production state and transition state.
It is given as,
Ea (rev) = Ea (fwd) − ΔHrxn
Given,
ΔH° = 83KJ
Ea (fwd) = 86 kJ/mol
Substituting the values above as:
Ea (rev) = 86 - 83
= 3 kJ
Therefore, the activation energy of the reverse reaction is 3 kJ.
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Zinc (Zn) has less than 34 protons, 30 to be exact, and is a transition metal in Group 12. Note: it is also called a "post-transition metal."
A carboxylic acid is named in the IUPAC system by replacing the -e in the name of the parent alkane with -<u>oic acid</u>
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<h3>What is carboxylic acid?</h3>
Carboxylic acid is an organic acid that contains a carboxyl group (C(=O)OH) attached to an R-group. The general formula of a carboxylic acid is R−COOH or R−CO2H, with R referring to the alkyl, alkenyl, aryl, or other group. Carboxylic acids occur widely. Important examples include the amino acids and fatty acids. Deprotonation of a carboxylic acid gives a carboxylate anion.
Carboxylic acids are commonly identified by their trivial names. They often have the suffix -ic acid. IUPAC-recommended names also exist; in this system, carboxylic acids have an -oic acid suffix. For example, butyric acid (C3H7CO2H) is butanoic acid by IUPAC guidelines. For nomenclature of complex molecules containing a carboxylic acid, the carboxyl can be considered position one of the parent chain even if there are other substituents, such as 3-chloropropanoic acid. Alternately, it can be named as a "carboxy" or "carboxylic acid" substituent on another parent structure, such as 2-carboxyfuran.
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