help with study guide, thank you! please help answer all questions :) 31) fluoroform (right) is more acidic than methan (left). What is the best explanation why?A) the inductively withdrawing effect of fluorine increases the acidity of the CH bondB) there are more resonance structures stabilizing the conjugate base of fluoroformC) HF bonds are more acidic than CH bondsD) fluoroform is sp2 hybridized and methane is sp3 hybridized. Sp2 CH bonds are more acidic thansp2 CH bonds32) Which side of the equilibrium is favored?A) leftB) rightC) equalI

Hey, since there are multiple questions posted, we will answer first question. If you want any specific question to be answered then please submit that question only or specify the question number in your message.Inductive effect is a permanent effect in saturated carbon chain compounds. Here, the group attached to carbon chain should have a tendency to release or withdraw electrons. +I effect arises due to the presence of electron donating groups. -I effect arises due to the presence of electron withdrawing groups such as F, Cl, Br, NO2 -I effect strengthen the acidity and +I effect weakens the acidity. Given compounds are CF3H and CH4. When the acidic hydrogen in CF3H is removed, CF3- anion is formed. When the acidic hydrogen in CH4 is removed, CH3- anion is formed. If the stability of the anion is more, then the acidity also will be more. Due to the inductively withdrawing effect of fluorine, CF3- anion will be more stable which increases the acidity of the C-H bond. Therefore, the best explanation for the more acidity of fluoroform than methane is the inductively withdrawing effect of fluorine increases the acidity of the C-H bond.