2a:["$","span",null,{"className":"font-heading text-xl font-semibold leading-snug text-primary","children":"a"}] 2f:Tdcc,molécula

\ce{H2C=CH-CH=CH2}

?2b:["$","div",null,{"className":"col-span-3 grid grid-cols-subgrid","children":[null,[["$","div",null,{"className":"col-span-2 text-[17px] leading-relaxed","children":[["$","div",null,{"className":"flow-root","children":[["$","span",null,{"className":"whitespace-pre-line","children":[["$","$1","0",{"children":"¿Cuántos enlaces "}],["$","span","1",{"className":"whitespace-nowrap","dangerouslySetInnerHTML":{"__html":"

\\sigma

"}}],["$","$1","2",{"children":" y "}],["$","span","3",{"className":"whitespace-nowrap","dangerouslySetInnerHTML":{"__html":"

\\pi

"}}],["$","$1","4",{"children":" hay en la "}],["$","span","5",{"className":"whitespace-nowrap","dangerouslySetInnerHTML":{"__html":"$2f"}}],"$L30"]}],"$L31"]}],"$L32"]}],"$L33"],null]}] 2c:["$","$1","1",{"children":[null,["$","div",null,{"className":"grid grid-cols-[minmax(1.25rem,max-content)_1.75rem_minmax(0,1fr)_0rem] gap-x-2 sm:grid-cols-[minmax(2.75rem,max-content)_2rem_minmax(0,1fr)_4rem] sm:gap-x-3","children":[["$","span",null,{"className":"font-heading text-xl font-semibold leading-snug text-primary","children":"b"}],["$","div",null,{"className":"col-span-3 grid grid-cols-subgrid","children":[null,[["$","div",null,{"className":"col-span-2 text-[17px] leading-relaxed","children":[["$","div",null,{"className":"flow-root","children":[["$","span",null,{"className":"whitespace-pre-line","children":[["$","$1","0",{"children":"Escriba las fórmulas moleculares correspondientes a las siguientes fórmulas estructurales semidesarrolladas e identifique cada compuesto como un alcano, un alqueno o un hidrocarburo aromático."}]]}],["$","span",null,{"className":"float-right ml-3 sm:hidden","children":["$","span",null,{"className":"whitespace-nowrap text-[13px] leading-none text-muted-foreground","children":"1,5 pts"}]}]]}],["$","div",null,{"className":"mt-4 flex flex-col gap-4","children":[null,[["$","div","d3f9cdaf9accd8ffe3bcb4d9bea94260c89667a756eaf728ee56a5863ca43992.jpg",{"className":"flex flex-wrap items-end justify-center gap-4","children":[["$","figure","d3f9cdaf9accd8ffe3bcb4d9bea94260c89667a756eaf728ee56a5863ca43992.jpg",{"className":"w-full max-w-[46%] sm:max-w-[31%]","children":[["$","img",null,{"src":"https://qryvyucllvwrritsgeua.supabase.co/storage/v1/object/public/selectividad-diagrams/d3f9cdaf9accd8ffe3bcb4d9bea94260c89667a756eaf728ee56a5863ca43992.jpg","alt":"","width":259,"height":195,"loading":"lazy","decoding":"async","style":{"maxWidth":259},"className":"mx-auto h-auto w-full select-none mix-blend-multiply"}],["$","figcaption",null,{"className":"mt-1.5 text-center text-[13px] leading-snug text-muted-foreground","children":["$","span",null,{"className":"whitespace-pre-line","children":[["$","$1","0",{"children":"Estructura de un hidrocarburo cíclico con dos dobles enlaces y un sustituyente metilo"}]]}]}]]}],["$","figure","4ef13dcd206da483240bcb3bebb84340861a7e658fa676aa5adb5a5fb623b88e.jpg",{"className":"w-full max-w-[46%] sm:max-w-[31%]","children":[["$","img",null,{"src":"https://qryvyucllvwrritsgeua.supabase.co/storage/v1/object/public/selectividad-diagrams/4ef13dcd206da483240bcb3bebb84340861a7e658fa676aa5adb5a5fb623b88e.jpg","alt":"","width":168,"height":151,"loading":"lazy","decoding":"async","style":{"maxWidth":168},"className":"mx-auto h-auto w-full select-none mix-blend-multiply"}],["$","figcaption",null,{"className":"mt-1.5 text-center text-[13px] leading-snug text-muted-foreground","children":["$","span",null,{"className":"whitespace-pre-line","children":[["$","$1","0",{"children":"Estructura de un alcano ramificado (isobutano)"}]]}]}]]}],["$","figure","5789cb7924c596168d6a97fb90a4750bfe17f350449228ca164e6074625239dc.jpg",{"className":"w-full max-w-[46%] sm:max-w-[31%]","children":[["$","img",null,{"src":"https://qryvyucllvwrritsgeua.supabase.co/storage/v1/object/public/selectividad-diagrams/5789cb7924c596168d6a97fb90a4750bfe17f350449228ca164e6074625239dc.jpg","alt":"","width":171,"height":189,"loading":"lazy","decoding":"async","style":{"maxWidth":171},"className":"mx-auto h-auto w-full select-none mix-blend-multiply"}],["$","figcaption",null,{"className":"mt-1.5 text-center text-[13px] leading-snug text-muted-foreground","children":["$","span",null,{"className":"whitespace-pre-line","children":[["$","$1","0",{"children":"Estructura de un anillo de benceno"}]]}]}]]}]]}]],[]]}]]}],["$","span",null,{"className":"hidden text-right tabular-nums sm:block pt-0.5 text-sm font-medium text-foreground/70","children":"1,5 pts"}]],null]}]]}]]}] 2d:null 2e:["$","nav",null,{"aria-label":"Navegación entre ejercicios del examen","className":"mx-auto mb-14 grid w-full max-w-3xl grid-cols-2 gap-3 px-4 sm:px-6","children":[["$","$L6",null,{"href":"/ejercicio/a47d4114-1eeb-446b-b4aa-f4e3760ae26e","className":"motion-surface group/sib flex flex-col gap-1 rounded-xl border border-border/70 bg-card/70 px-4 py-3 hover:border-foreground/20 hover:bg-card hover:shadow-sm hover:shadow-foreground/5 focus-visible:outline-none focus-visible:ring-2 focus-visible:ring-ring/60 items-start text-left","children":[["$","span",null,{"className":"inline-flex items-center gap-1 text-[10px] font-semibold uppercase tracking-[0.2em] text-muted-foreground","children":[["$","svg",null,{"viewBox":"0 0 24 24","fill":"none","stroke":"currentColor","strokeWidth":2,"strokeLinecap":"round","strokeLinejoin":"round","aria-hidden":"true","className":"size-3","children":[["$","path",null,{"d":"M19 12H5"}],["$","path",null,{"d":"m11 18-6-6 6-6"}]]}],"Anterior",null]}],["$","span",null,{"className":"font-heading text-sm font-semibold tracking-tight text-foreground transition-colors duration-150 group-hover/sib:text-primary sm:text-base","children":"Ejercicio 8"}]]}],["$","$L6",null,{"href":"/ejercicio/37e9b67c-f6ff-4763-921c-9f3e88571a6b","className":"motion-surface group/sib flex flex-col gap-1 rounded-xl border border-border/70 bg-card/70 px-4 py-3 hover:border-foreground/20 hover:bg-card hover:shadow-sm hover:shadow-foreground/5 focus-visible:outline-none focus-visible:ring-2 focus-visible:ring-ring/60 items-end text-right","children":[["$","span",null,{"className":"inline-flex items-center gap-1 text-[10px] font-semibold uppercase tracking-[0.2em] text-muted-foreground","children":[null,"Siguiente",["$","svg",null,{"viewBox":"0 0 24 24","fill":"none","stroke":"currentColor","strokeWidth":2,"strokeLinecap":"round","strokeLinejoin":"round","aria-hidden":"true","className":"size-3","children":[["$","path",null,{"d":"M5 12h14"}],["$","path",null,{"d":"m13 6 6 6-6 6"}]]}]]}],["$","span",null,{"className":"font-heading text-sm font-semibold tracking-tight text-foreground transition-colors duration-150 group-hover/sib:text-primary sm:text-base","children":"Ejercicio 10"}]]}]]}]