Answer:
answer #1 used throughout the world to power devices, appliances and methods of transportation utilized in daily life. To make things operate, electrical energy must be emitted from energy sources such as power plants, to enable an object to consume the power it needs to function. ((if you want to cut it down short use the two first sentences))
answer #2 We get solar heat energy from the sun, and sunlight can also be used to produce electricity from solar
Explanation:
Answer:
ΔH rxn = -1010 kJ/molC₂H₂
Explanation:
To obtain the enthalpy change for a reaction from bond energies what we do is to make an inventory of the bonds broken and formed for the balanced chemical reaction:
C₂H₂ + 5/2O₂ ⇒ 2CO₂ + H₂O
Bond Broken Bonds Formed
2 C-H + 1 C≡C + 5/2 O=O 4C=O + 2 H-O
Enthalpy bonds broken:
2 mol (456 kJ/mol)+ 1 mol (962 kJ/mol) + 5/2 mol (499 kJ/mol) = 3121.5 kJ
Enthalpy bond formed:
4 mol (802 kJ/mol) + 2 mol (462 kJ/mol) = 4132.0 kJ
ΔH rxn = H broken - H formed = 3121.5 kJ - 4132.0 kJ = - 1010 kJ (per mol C₂H₂ )
Answer:Acid catalyst is needed to increase the electrophilicity of Carbonyl group of Carboxylic acid as alcohol is a weak nucleophile.
Alternatively esters can be synthesised by converting carboxylic acid into acyl chloride using thionyl chloride(SOCl_{2} and then further treating acyl chloride with alcohol.
Carboxylic acid and esters can be easily distinguished on the basis of IR as carboxylic acid would contain a broad intense peak in 2500-3200cm_{-1} corresponding to OH stretching frequency whereas esters would not contain any such broad intense peak.
Alcohol and esters can also be distinguished using IR as alcohols would contain a broad intense peak at around 3200-3600cm_{-1}
Explanation: For the synthesis of esters using alcohol and carboxylic acid we need to add a little amount of acid in the reaction . The acid used here increases the electrophilicity of carbonyl carbon and hence makes it easier for a weaker nucleophile like alcohol to attack the carbonyl carbon of acid.
The oxygen of the carbonyl group is protonated using the acidic proton which leads to the generation of positive charge on the oxygen. The positive charge generated is delocalised over the whole acid molecule and hence the electrophilicity of carbonyl group is increased. Kindly refer attachment for the structures.
If we simply mix the acid and alcohol then no appreciable reaction would take place between them and ester formation would not take place because the carboxylic acid in that case is not a good electrophile whereas alcohol is also not a very strong nucleophile which can attack the carbonyl group.
Alternatively we can use thionyl chloride or any other reagent which can convert the carboxylic acid into acyl chloride. Acyl chloride is very elctrophilic and alcohol can very easily attack the acyl chloride and esters could be synthesized.
The carboxylic acid and ester can very easily be distinguished on the basis of broad intense OH stretching frequency peak at around 2500-3200cm_{-1} . The broad intense OH stretching frequency peak is present in carboxylic acids as they contain OH groups and absent in case of esters .
Likewise esters and alcohols can also be distinguished on the basis IR spectra as alcohols will have broad intense spectra at around 3200-3600cm_{-1}corresponding to OH stretching frequency whereas esters will not have any such peak. Rather esters would be having a Carbonyl stretching frequency at around 1720-1760
Answer:
We can use heat = mcΔT to determine the amount of heat, but first we need to determine ΔT. Because the final temperature of the water is 55°C and the initial temperature is 20.0°C, ΔT is as follows:
ΔT = Tfinal − Tinitial = 55.0°C − 20.0°C = 35.0°C
given the specific heat of water as 1 cal/g·°C. Substitute the known values into heat = mcΔT and solve for amount of heat:
= heat=(75.0 g)(1 cal/ g· °C )(35.0°C) =
= 75x1x35=2625 cal
'cause alphe-particle which was +ve charge, get repulsion from the atom, so he deducted that.......