False, atoms can not be created that way
Answer:
Adenosine diphosphate (ADP) and inorganic phosphate
Answer:
51.2g of CO2
Explanation:
The first step is to balance the reaction equation as shown in the solution attached. Without balancing the reaction equation, one can never obtain the correct answer! Then obtain the masses of octane reacted and carbon dioxide produced from the stoichiometric equation. After that, we now compare it with what is given as shown in the image attached.
Answer:
B. Salt, NaCl, is produced by the process of evaporation of seawater or brine. If the surface area of the water is increased, the same volume of water evaporates faster.
C. The Haber process combines hydrogen and nitrogen to make ammonia. The two gases are passed through a reactor under pressure and at high temperatures. If iron is added to the reactor, the yield of ammonia increases.
Explanation:
Evaporation of water is responsible for the production of sodium chloride also known as table salt. Sodium and chlorine are present in water. When more evaporation of water occurs, sodium and chlorine come close together forming sodium chloride. Haber process is responsible for the production of ammonia which is used as fertilizer. For speed up the process, catalyst is used such as iron in order to complete the reaction in less time. Iron binds hydrogen and nitrogen with each other.
Answer:
None of these
Explanation:
Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.
Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :
Step -1 : Generation of stable carbocation.
Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.
Step-2: Attack of the ring to the carbocation
The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.
The product formed is shown in mechanism does not mention in any of the options.
So, None of these is the answer