
Interpretation:
The name of the molecule should be identified.
Concept introduction:
According to the nomenclature, when two nonmetals are present in the given compound the name of the compound is given as follows, For example, HCl. According to the name of the compound, first give the name for the hydrogen followed by the second element, changing the ending of its name to –ide. Chlorine called as chloride. Therefore HCl is hydrogen chloride. Similarly, HI is hydrogen iodide. SiC is silicon carbide.
One pair of elements to form several different binary molecular compounds. In these cases, using of Greek prefixes to denote the number of atoms of each element present.
Greek prefixes are given below,
If prefix mono substituted is generally omitted for the first element. For example, SO2 is named sulfur dioxide, is not monosulfur dioxide. Moreover, only one atom in a prefix for the first element, no needs to mention mono or di etc. In addition, for ease of pronunciation, we usually eliminate the last letter of a prefix that ends in o or a when naming an oxide. Thus, N2O5 is dinitrogen pentoxide, rather than dinitrogen pentaoxide.
If any halogens are present in the molecule in suffix, the name of the halogens as follows.

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Chapter 5 Solutions
Chemistry: Atoms First
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- What does the phrase 'fit for purpose' mean in relation to analytical chemistry? Please provide examples too.arrow_forwardFor each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects Resonance Effects Overall Electron-Density × NO2 ○ donating O donating O withdrawing O withdrawing O electron-rich electron-deficient no inductive effects O no resonance effects O similar to benzene E [ CI O donating withdrawing O no inductive effects Explanation Check ○ donating withdrawing no resonance effects electron-rich electron-deficient O similar to benzene © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accesarrow_forwardUnderstanding how substituents activate Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation HN NH2 Check X (Choose one) (Choose one) (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Aarrow_forward
- Identifying electron-donating and electron-withdrawing effects on benzene For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Inductive Effects Resonance Effects Overall Electron-Density Molecule CF3 O donating O donating O withdrawing O withdrawing O no inductive effects O no resonance effects electron-rich electron-deficient O similar to benzene CH3 O donating O withdrawing O no inductive effects O donating O withdrawing Ono resonance effects O electron-rich O electron-deficient O similar to benzene Explanation Check Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward* Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forwardDraw TWO general chemical equation to prepare Symmetrical and non-Symmetrical ethers Draw 1 chemical reaction of an etherarrow_forward
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