Answer:
The correct option is: c. petroleum jelly, d. Polyethylene glycol 4000/600 mixture
Explanation:
Topical medications are used for the treatment of ailments and include ointments, gels, lotions creams etc. that can applied directly on the surface of the body i.e. skin.
An ointment base medication gets rapidly absorbed into the skin. Some of the examples of <u>ointment bases</u> include water-soluble bases: <u>polyethylene glycol</u>, hydrocarbon bases: <u>petroleum jelly</u>, paraffin wax.
Answer:
CuBr₂(aq) + Pb(CH₃COO)₂(aq) → Cu(CH₃COO)₂(aq) + PbBr₂ (s)↓
Explanation:
We identify the reactants:
CuBr₂ and Pb(CH₃COO)₂
The products will be: Cu(CH₃COO)₂ and PbBr₂
You may know these information:
Salts from acetate are soluble.
Bromide can make solid salts with these cations: Ag⁺, Pb²⁺, Hg₂²⁺, Cu⁺
PbBr₂ is formed, so this will be our precipitate
The equation is:
CuBr₂(aq) + Pb(CH₃COO)₂(aq) → Cu(CH₃COO)₂(aq) + PbBr₂ (s)↓
Answer:atomic mass, neutrons in the nucleus
Explanation: because I remember from when I took honors chemistry last year we learned about this and it’s called the atomic mass when looking at an atom and the neutrons in the nucleus are effected by it.
Answer:
The three-step synthesis of trans-2-pentene from acetylene is as follows.
<u>Step -1:</u> Formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkanes.
<u>Step -2:</u> Formation terminal alkyne to nonterminal alkynes.
<u>Step -3:</u> Formation of trans-pent - 2-pent-ene by reduction.
Explanation:
Synthesis of trans-pent-2-yne from ethyne takes place is mainly a three step synthesis which involves formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkane. Second step involves the further alkylation of terminal alkynes to higher order nonterminal alkynes and the third step involves the formation of trans-2-ene by dissolving reduction method.
The chemical reaction of each step of chemical reactions is as follows.
Answer:
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Explanation:
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