What amount of heat absorbs 50 g of steel (ce = 0.115 cal / g. ° C) that
does its temperature vary by 25 ° C?
Answer:
143.75cal
Explanation:
Given parameters:
Mass of steel = 50g
Specific heat capacity of the steel = 0.115cal/g°C
Temperature = 25°C
Unknown:
Amount of heat = ?
Solution:
The amount of heat to cause this temperature change is dependent on mass and specific heat capacity of the substance.
Amount of heat = m C (ΔT)
m is the mass
c is the specific heat capacity
ΔT is the temperature change
Now insert the parameters and solve;
Amount of heat = 50 x 0.115 x 25
Amount of heat = 143.75cal
Answer:
Fe₃Si₇
Explanation:
In order to determine the empirical formula, we have to follow a series of steps.
Step 1: Determine the percent composition
Fe: 46.01%
Si: 53.99%
Step 2: Divide each percentage by the atomic mass of the element
Fe: 46.01/55.85 = 0.8238
Si: 53.99/28.09 = 1.922
Step 3: Divide all the numbers by the smallest one
Fe: 0.8238/0.8238 = 1
Si: 1.922/0.8238 = 2.33
Step 4: Multiply by numbers that make the coefficients whole.
Fe: 1 × 3 = 3
Si: 2.33 × 3 = 7
The empirical formula is Fe₃Si₇.
Answer:
2Al(NO3)3 + 3H2SO4 → Al2(SO4)3 + 6HNO3
Explanation:
i just looked up how to balance it, i dont really know how to balance it exactly
We all have favorite things we eat, watch on TV, hobbies we like, places we love to travel, etc. Either write or draw picture of you doing one of your favorite things. Then follow these directions...
Answer:
a. electrophilic aromatic substitution
b. nucleophilic aromatic substitution
c. nucleophilic aromatic substitution
d. electrophilic aromatic substitution
e. nucleophilic aromatic substitution
f. electrophilic aromatic substitution
Explanation:
Electrophilic aromatic substitution is a type of chemical reaction where a hydrogen atom or a functional group that is attached to the aromatic ring is replaced by an electrophile. Electrophilic aromatic substitutions can be classified into five classes: 1-Halogenation: is the replacement of one or more hydrogen (H) atoms in an organic compound by a halogen such as, for example, bromine (bromination), chlorine (chlorination), etc; 2- Nitration: the replacement of H with a nitrate group (NO2); 3-Sulfonation: the replacement of H with a bisulfite (SO3H); 4-Friedel-CraftsAlkylation: the replacement of H with an alkyl group (R), and 5-Friedel-Crafts Acylation: the replacement of H with an acyl group (RCO). For example, the Benzene undergoes electrophilic substitution to produce a wide range of chemical compounds (chlorobenzene, nitrobenzene, benzene sulfonic acid, etc).
A nucleophilic aromatic substitution is a type of chemical reaction where an electron-rich nucleophile displaces a leaving group (for example, a halide on the aromatic ring). There are six types of nucleophilic substitution mechanisms: 1-the SNAr (addition-elimination) mechanism, whose name is due to the Hughes-Ingold symbol ''SN' and a unimolecular mechanism; 2-the SN1 reaction that produces diazonium salts 3-the benzyne mechanism that produce highly reactive species (including benzyne) derived from the aromatic ring by the replacement of two substituents; 4-the free radical SRN1 mechanism where a substituent on the aromatic ring is displaced by a nucleophile with the formation of intermediary free radical species; 5-the ANRORC (Addition of the Nucleophile, Ring Opening, and Ring Closure) mechanism, involved in reactions of metal amide nucleophiles and substituted pyrimidines; and 6-the Vicarious nucleophilic substitution, where a nucleophile displaces an H atom on the aromatic ring but without leaving groups (such as, for example, halogen substituents).
