Which of the following statements regarding hydrogen bonding in secondary structures is true? Group of answer choices Both α-hel
1 answer:
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<h2>Hey There!</h2><h2>_____________________________________</h2><h2>Answer:</h2>
Calorimeter is device used for the measurement of heat. In a calorimeter we can use the temperature change of water to quantify an amount of heat. A calorimeter just captures all the energy released (or absorbed) by a reaction in the water. So Option A and B are wrong as calorimeter don't have anything to do with providing the heat or letting the the heat in, as it is the insulated calorimeter too.
<h2>_____________________________________</h2><h2>Energy in the reaction:</h2>In the formation of any bond there is equal amount of heat required as to break that bond. It means Energy released in the making of bond is equal to the energy required in the breaking of the bond. So Option D is wrong as it says we need more energy in making then breaking.
<h2>_____________________________________</h2><h2>Enthalpy:</h2>Enthalpy is the total heat content of the system. As we provide energy to the reactants and the product is formed, so The enthalpy(heat content) of product is more than the Enthalpy of the reactant, Thus Option C is correct.
Enthalpy is denoted by H or Q, its formula is,
H = U + PV
Where,
U is internal energy
PV is equals to Work done ; P = Pressure, V = Volume
<h2>_____________________________________</h2><h2>Best Regards,</h2><h2>'Borz'</h2><h2> </h2>Answer:
Reaction mechanism has been given below
Explanation:
- Propanoyl chloride contains an electrophilic carbonyl center to give nucleophilic acyl substitution reaction by removing Cl group with a strong nucleophile like methylmagnesium bromide.
- Two equivalent of methyl magnesium bromide react with cabonyl center followed by protonation of negatively charged oxygen atom gives 2-methyl-2-butanol.
- In the first step, nucleophilic acyl substituion occurs. In the second step, nucleophilic addition occurs. In the third step, protonation occurs.
- Reaction mechanism has been shown below.
