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- Rank the molecules in decreasing (strongest to weakest) acidity. Include resonance structures if necessary and explain reasoning for rank.Which of the following compounds is the stronger base? Explain. or NH3 is a v base than NCI3. This is due to the difference in the electron withdrawing strength of Cl compared with H. v is more electronegative than and will v more electron density v the nitrogen than Thus, the nitrogen atom in NCI3 has a v positive charge than it does in NH3. The v positive charge means that is v difficult to add H* to NCI3 than it is to add H* to NH3. Is the compound Sb(OH)5 likely to be acidic, basic, or neutral in water? Justify your answer. Phosphorus and arsenic form acids of the form X(OH)n, so one would predict that antimony would be similar as it is in the same family. Based in the number of OH groups present, it should be However, antimony hydroxides are not stable and form oxides which are known to be amphoteric. Thus, Sb(OH)6 is in fact more likely to beLabel each molecule according to increasing acidity with 1 as the weakest and 4 as the strongest based on their structure. Explain.
- Rank the following compounds in terms of increasing acidity (least acidic first). Explain your ranking. Making sure to say which hydrogen in each molecule is the most acidic, and discuss the relative stability of the conjugate bases.Predict the product for the following reaction. H NaOH/H,O A II II I V IV 1) I 2) || 3) |II O 4) IV 5) VExplain the difference in acidity of the following compounds.
- Rank the indicated atoms from the most (1) to the least (3) basic. C ANH NH2 A B1. Rank, with explanation the compounds in each group below in order of increasing acidity. (i) CI Br СООН СООН COOH (ii) OH LOH HO O2N (ii) CO,H CO,H O,N- CO2H O2N-Explain why phenol is more acidic than alcohols by considering the resonance effect anddrawing the resonance structures of phenoxide ions.
- which of the following compounds is the strongest acid?Why is ths the correct order in terms of reactvity. I throught fluroine has more electronegatvity so its the most acidic.what causes an alkane, alkene, and alkyne differ in acidity Please explain. I understand that the more S characteristic of an orbital the more stable but can you explain further and give an example