
(a)
Interpretation:
Formula of sulfur tetrafluoride has to be written.
Concept Introduction:
Two or more nonmetals combine to form molecular compounds. The naming of molecular compound is given by following two rules.
- Element that is present in far left of the periodic table appears in the name first.
- Element that is closer to bottom within any of the group appears in the name first.
Numerical prefixes are used in case of molecular compounds to mention how many times the atom of same elements occurs in the formula. Prefix mono is not used for the first element while for the second element it is used.
From the name of molecular compound, the molecular formula can be obtained by considering the name of the first element and second element along with the prefix. The prefix represents the number of atoms of same element is present in the molecular formula. This prefix is entered in subscript in molecular formula after the
(b)
Interpretation:
Formula of nitrogen trichloride has to be written.
Concept Introduction:
Refer part (a).
(c)
Interpretation:
Formula of dinitrogen pentoxide has to be written.
Concept Introduction:
Refer part (a).
(d)
Interpretation:
Formula of chlorine trifluoride has to be written.
Concept Introduction:
Refer part (a).

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Chapter 2 Solutions
Chemistry: Principles and Practice
- Draw the Fischer projection of D-fructose. Click and drag to start drawing a structure. Skip Part Check AP 14 tv SC F1 F2 80 F3 a F4 ! 2 # 3 CF F5 75 Ax MacBook Air 894 $ 5olo % Λ 6 > W F6 K F7 &arrow_forwardConsider this step in a radical reaction: Y What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. ionization propagation initialization passivation none of the abovearrow_forward22.16 The following groups are ortho-para directors. (a) -C=CH₂ H (d) -Br (b) -NH2 (c) -OCHS Draw a contributing structure for the resonance-stabilized cation formed during elec- trophilic aromatic substitution that shows the role of each group in stabilizing the intermediate by further delocalizing its positive charge. 22.17 Predict the major product or products from treatment of each compound with Cl₁/FeCl₂- OH (b) NO2 CHO 22.18 How do you account for the fact that phenyl acetate is less reactive toward electro- philic aromatic substitution than anisole? Phenyl acetate Anisole CH (d)arrow_forward
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- V Consider this step in a radical reaction: Br: ? What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. ⚫ionization termination initialization neutralization none of the abc Explanation Check 80 Ο F3 F1 F2 2 F4 01 % do5 $ 94 #3 X 5 C MacBook Air 25 F5 F6 66 ©2025 ˇ F7 29 & 7 8arrow_forwardShow how to convert ethyl benzene to (a) 2,5-dichlorobenzoic acid and (b) 2,4-dichlorobenzoic acid.arrow_forwardno aiarrow_forward
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