this would have a charge of 4 plus
Answer : The final temperature of the metal block is, 
Explanation :
As we know that,
![m_1\times c_1\times (T_{final}-T_1)=-[m_2\times c_2\times (T_{final}-T_2)]](https://tex.z-dn.net/?f=m_1%5Ctimes%20c_1%5Ctimes%20%28T_%7Bfinal%7D-T_1%29%3D-%5Bm_2%5Ctimes%20c_2%5Ctimes%20%28T_%7Bfinal%7D-T_2%29%5D)
.................(1)
where,
q = heat absorbed or released
= mass of aluminum = 55 g
= mass of water = 0.48 g
= final temperature = ?
= temperature of aluminum =
= temperature of water =
= specific heat of aluminum = 
= specific heat of water= 
Now put all the given values in equation (1), we get
![55g\times 0.900J/g^oC\times (T_{final}-25)^oC=-[0.48g\times 4.184J/g^oC\times (T_{final}-25)^oC]](https://tex.z-dn.net/?f=55g%5Ctimes%200.900J%2Fg%5EoC%5Ctimes%20%28T_%7Bfinal%7D-25%29%5EoC%3D-%5B0.48g%5Ctimes%204.184J%2Fg%5EoC%5Ctimes%20%28T_%7Bfinal%7D-25%29%5EoC%5D)
Thus, the final temperature of the metal block is,
Answer:
false
Explanation:
because it's just a physical change, the matter won't be changed.
Hope this might help you! I don't know if this is going to be right on everything, but it's a anwser
Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
